Acridarsine,10-phenyl-

    WARNING: This product is for research use only, not for human or veterinary use.

MedKoo CAT#: 591005

CAS#: 28660-45-9

Description: Acridarsine,10-phenyl- is a biochemcial.

Chemical Structure

img
Acridarsine,10-phenyl-
CAS# 28660-45-9
Instruction

Theoretical Analysis

MedKoo Cat#: 591005
Name: Acridarsine,10-phenyl-
CAS#: 28660-45-9
Chemical Formula: C19H13As
Exact Mass: 316.02
Molecular Weight: 316.230
Elemental Analysis: C, 72.16; H, 4.14; As, 23.69

Price and Availability

This product is not in stock, which may be available by custom synthesis. For cost-effective reason, minimum order is 1g (price is usually high, lead time is 2~3 months, depending on the technical challenge). Quote less than 1g will not be provided. To request quote, please email to sales @medkoo.com or click below button.
Note: Price will be listed if it is available in the future.

Request quote for custom synthesis

Synonym: Acridarsine,10-phenyl-

IUPAC/Chemical Name: Acridarsine,10-phenyl-

InChi Key: YDRNCDWYRCHVQJ-UHFFFAOYSA-N

InChi Code: InChI=1S/C19H13As/c1-2-8-14(9-3-1)19-15-10-4-6-12-17(15)20-18-13-7-5-11-16(18)19/h1-13H

SMILES Code: C12=[As]C3=CC=CC=C3C(C4=CC=CC=C4)=C1C=CC=C2

Appearance: Solid powder

Purity: >98% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility: Soluble in DMSO

Shelf Life: >2 years if stored properly

Drug Formulation: This drug may be formulated in DMSO

Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code: 2934.99.9001

More Info:

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 316.23 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
In vitro protocol:
In vivo protocol:

Molarity Calculator

Calculate the mass, volume, or concentration required for a solution.
=
x
x
g/mol

*When preparing stock solutions always use the batch-specific molecular weight of the product found on the vial label and SDS / CoA (available online).

Reconstitution Calculator

The reconstitution calculator allows you to quickly calculate the volume of a reagent to reconstitute your vial. Simply enter the mass of reagent and the target concentration and the calculator will determine the rest.

=
÷

Dilution Calculator

Calculate the dilution required to prepare a stock solution.
x
=
x

1: Carballeira NM, Morales-Guzman C, Alvarez-Benedicto E, Torres-Martinez Z, Delgado-Reyes Y, Griebenow KH, Tinoco AD, Reguera RM, Perez-Pertejo Y, Carbajo-Andres R, Balana-Fouce R. First Total Synthesis of -Phenyl 6 Fatty Acids and their Leishmanicidal and Anticancer Properties. Curr Top Med Chem. 2018 May 16. doi: 10.2174/1568026618666180516125056. [Epub ahead of print] PubMed PMID: 29766807.

2: Christensen JA, Phelan BT, Chaudhuri S, Acharya A, Batista VS, Wasielewski MR. Phenothiazine Radical Cation Excited States as Super-oxidants for Energy-Demanding Reactions. J Am Chem Soc. 2018 Apr 18;140(15):5290-5299. doi: 10.1021/jacs.8b01778. Epub 2018 Apr 6. PubMed PMID: 29589754.

3: Matsuo Y, Okada H, Kondo Y, Jeon I, Wang H, Yu Y, Matsushita T, Yanai M, Ikuta T. Anthracene-Based Organic Small-Molecule Electron-Injecting Material for Inverted Organic Light-Emitting Diodes. ACS Appl Mater Interfaces. 2018 Apr 11;10(14):11810-11817. doi: 10.1021/acsami.8b00603. Epub 2018 Mar 30. PubMed PMID: 29485261.

4: Yang J, Zhen X, Wang B, Gao X, Ren Z, Wang J, Xie Y, Li J, Peng Q, Pu K, Li Z. The influence of the molecular packing on the room temperature phosphorescence of purely organic luminogens. Nat Commun. 2018 Feb 26;9(1):840. doi: 10.1038/s41467-018-03236-6. PubMed PMID: 29483501; PubMed Central PMCID: PMC5826932.

5: Sun W, Zhou N, Xiao Y, Wang S, Li X. A Novel Spiro[acridine-9,9'-fluorene] Derivatives Containing Phenanthroimidazole Moiety for Deep-Blue OLED Application. Chem Asian J. 2017 Dec 5;12(23):3069-3076. doi: 10.1002/asia.201701292. Epub 2017 Oct 30. PubMed PMID: 28984424.

6: Chansaenpak K, Yang M, Gabbaï FP. Attempted synthesis of ortho-phenylene phosphino-tritylium cations. Philos Trans A Math Phys Eng Sci. 2017 Aug 28;375(2101). pii: 20170007. doi: 10.1098/rsta.2017.0007. PubMed PMID: 28739965; PubMed Central PMCID: PMC5540840.

7: Yang LJ, Liao HX, Bai M, Huang GL, Luo YP, Niu YY, Zheng CJ, Wang CY. One new cytochalasin metabolite isolated from a mangrove-derived fungus Daldinia eschscholtzii HJ001. Nat Prod Res. 2018 Jan;32(2):208-213. doi: 10.1080/14786419.2017.1346641. Epub 2017 Jun 28. PubMed PMID: 28658974.

8: Ramesh K, Satyanarayana G. A Domino Palladium-Catalyzed Cyclization: One-Pot Synthesis of 4b-Alkyl-10-phenyl-4b,5-dihydroindeno[2,1-a]indenes via Carbopalladation Followed by C-H Activation. J Org Chem. 2017 Apr 21;82(8):4254-4264. doi: 10.1021/acs.joc.7b00254. Epub 2017 Apr 10. PubMed PMID: 28358198.

9: Alicea-Matías E, Soderquist JA. Asymmetric Propargylboration of Aldimines and Ketimines with the Borabicyclo[3.3.2]decanes: Novel Entries to Allenyl Carbinamines, Amino Acids, and Their α-Methyl Counterparts. Org Lett. 2017 Jan 20;19(2):336-339. doi: 10.1021/acs.orglett.6b03506. Epub 2017 Jan 3. PubMed PMID: 28045535.

10: Guo L, Li KF, Zhang X, Cheah KW, Wong MS. Highly Efficient Multiphoton-Pumped Frequency-Upconversion Stimulated Blue Emission with Ultralow Threshold from Highly Extended Ladder-Type Oligo(p-phenylene)s. Angew Chem Int Ed Engl. 2016 Aug 26;55(36):10639-44. doi: 10.1002/anie.201604064. Epub 2016 Aug 3. PubMed PMID: 27485210.

11: Kang S, Lee H, Kim B, Park Y, Park J. Synthesis and Property of New Propeller Shaped Emitting Materials for Organic Light-Emitting Devices. J Nanosci Nanotechnol. 2016 Mar;16(3):3102-5. PubMed PMID: 27455768.

12: Lam J, Günther BA, Farrell JM, Eisenberger P, Bestvater BP, Newman PD, Melen RL, Crudden CM, Stephan DW. Chiral carbene-borane adducts: precursors for borenium catalysts for asymmetric FLP hydrogenations. Dalton Trans. 2016 Oct 21;45(39):15303-15316. Epub 2016 Jul 7. PubMed PMID: 27383522.

13: Esdaile LJ, Rintoul L, Goh MS, Merahi K, Parizel N, Wellard RM, Choua S, Arnold DP. Nickel(II) meso-Hydroxyporphyrin Complexes Revisited: Palladium-Catalysed Synthesis, Electronic Structures of Derived Oxy Radicals, and Oxidative Coupling to a Dioxoporphodimethene Dyad. Chemistry. 2016 Mar 1;22(10):3430-3446. doi: 10.1002/chem.201504252. Epub 2016 Feb 2. PubMed PMID: 26833709.

14: Kim C, Yoon JY, Lee SJ, Lee HW, Kim YK, Yoon SS. Various Blue Emitting Materials Based on Pyrene Derivatives for Organic Light-Emitting Diodes. J Nanosci Nanotechnol. 2015 Jul;15(7):5246-9. PubMed PMID: 26373116.

15: Hebié S, Dimé AK, Devillers CH, Lucas D. Electrochemistry as an attractive and effective tool for the synthesis and immobilization of porphyrins on an electrode surface. Chemistry. 2015 May 26;21(22):8281-9. doi: 10.1002/chem.201404314. Epub 2015 Apr 17. PubMed PMID: 25891408.

16: Liu XY, Liang F, Cui LS, Yuan XD, Jiang ZQ, Liao LS. Effective host materials for blue/white organic light-emitting diodes by utilizing the twisted conjugation structure in 10-phenyl-9,10-dihydroacridine block. Chem Asian J. 2015 Jun;10(6):1402-9. doi: 10.1002/asia.201500235. Epub 2015 May 5. PubMed PMID: 25871535.

17: Nishibori E, Aoyagi S, Sakata M, Sakamoto R, Nishihara H. Crystal structure of (Z)-1-(ferrocenylethyn-yl)-10-(phenyl-imino)-anthracen-9(10H)-one from synchrotron X-ray powder diffraction. Acta Crystallogr Sect E Struct Rep Online. 2014 Nov 26;70(Pt 12):573-6. doi: 10.1107/S1600536814025252. eCollection 2014 Dec 1. PubMed PMID: 25552995; PubMed Central PMCID: PMC4257377.

18: Toba R, Gotoh H, Sakakibara K. Scavenging and characterization of short-lived radicals using a novel stable nitroxide radical with a characteristic UV-vis absorption spectrum. Org Lett. 2014 Aug 1;16(15):3868-71. doi: 10.1021/ol501328k. Epub 2014 Jul 14. PubMed PMID: 25019641.

19: Shah VB, Biswas P. Aerosolized droplet mediated self-assembly of photosynthetic pigment analogues and deposition onto substrates. ACS Nano. 2014 Feb 25;8(2):1429-38. doi: 10.1021/nn405251h. Epub 2014 Jan 14. PubMed PMID: 24422474.

20: Jayasinghe S, Venukadasula PK, Hanson PR. An efficient, modular approach for the synthesis of (+)-strictifolione and a related natural product. Org Lett. 2014 Jan 3;16(1):122-5. doi: 10.1021/ol403110p. Epub 2013 Dec 2. PubMed PMID: 24294936; PubMed Central PMCID: PMC4179430.