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155885-64-6

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155885-64-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 155885-64-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,8,8 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 155885-64:
(8*1)+(7*5)+(6*5)+(5*8)+(4*8)+(3*5)+(2*6)+(1*4)=176
176 % 10 = 6
So 155885-64-6 is a valid CAS Registry Number.

155885-64-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2H-indol-3-yl)-9H-pyrido[3,4-b]indole

1.2 Other means of identification

Product number -
Other names 9H-Pyrido(3,4-b)indole,1-(1H-indol-3-yl)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:155885-64-6 SDS

155885-64-6Downstream Products

155885-64-6Relevant articles and documents

New syntheses of the marine alkaloids eudistomins D and U

Rocca,Rocca, Patrick,Marsais,Marsais, Francis,Godard,Godard, Alain,Queguiner,Queguiner, Guy,Adams,Adams, Luqman,Alo,Alo, Babajide

, p. 7085 - 7088 (1995)

Short and convergent syntheses of eudistomins U and D are reported. The approach is based on a convergent methodology which involves such reactions as metalation and heteroring cross-coupling.

Manipulation of Water for Diversified Functionalization of Tetrahydro-β-carbolines (THβCs) with Indoles

Xu, Dekang,Ye, Fu,Ye, Jinxiang,Gao, Yu,Chen, Haijun

, p. 6160 - 6163 (2019)

Water plays a crucial role in organic synthesis. However, diversified functionalization manipulated by water is still rare and remains unexplored. Herein, we report the first water-manipulated protocol to achieve the diversified functionalization of tetrahydro-β-carbolines (THβCs) in an open flask at room temperature that exhibit a broad functional-group tolerance. More water leads to monoarylation, while less water leads to diarylation. Further one-step transformation afforded oxidized bis(indolyl)methanes, eudistomin U, and the related derivatives in satisfactory yields.

Efficient synthesis of eudistomin U and evaluation of its cytotoxicity

Roggero, Chad M.,Giulietti, Jennifer M.,Mulcahy, Seann P.

, p. 3549 - 3551 (2014)

Eudistomin U is a member of a subclass of naturally occurring indole alkaloids known as β-carbolines. These molecules are reported to have diverse biological activity and high binding affinity to DNA, which make them attractive targets for total synthesis

Application of metal free aromatization to total synthesis of perlolyrin, flazin, eudistomin U and harmane

Santhanam, Srinath,Ramu, Abinaya,Baburaj, Baskar,Kalpatu Kuppusamy, Balasubramanian

, p. 2121 - 2127 (2020/03/04)

Application of our recently reported metal free reaction conditions to the total synthesis of the four different and selective biologically interesting β-carboline natural products is reported. Using this simple methodology, flazin, perlolyrine, eudistomin U and harmane containing heteroaryl and alkyl substituents at C1 position were synthesized in good yields. (Figure presented.).

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