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219959-85-0

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219959-85-0 Usage

Chemical Properties

Dark Yellow Solid

Uses

Different sources of media describe the Uses of 219959-85-0 differently. You can refer to the following data:
1. A mutagenic compound
2. A mutagenic compound.

Check Digit Verification of cas no

The CAS Registry Mumber 219959-85-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,9,5 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 219959-85:
(8*2)+(7*1)+(6*9)+(5*9)+(4*5)+(3*9)+(2*8)+(1*5)=190
190 % 10 = 0
So 219959-85-0 is a valid CAS Registry Number.
InChI:InChI=1/C17H11N3O2/c21-20(22)13-7-5-12(6-8-13)19-16-4-2-1-3-14(16)15-9-10-18-11-17(15)19/h1-11H

219959-85-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-(4-nitrophenyl)pyrido[3,4-b]indole

1.2 Other means of identification

Product number -
Other names Nitrophenylnorharman

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:219959-85-0 SDS

219959-85-0Downstream Products

219959-85-0Relevant articles and documents

Chemical confirmation of the structure of a mutagenic aminophenylnorharman, 9-(4'-aminophenyl)-9H-pyrido[3,4-b]indole : An authentic synthesis of 9-(4'nitrophenyl)-9H- pyrido[3,4-b]indole as its relay compound

Murakami, Yasuoki,Imai, Nobuyuki,Miura, Tsuyoshi,Sugimura, Takashi,Wakabayashi, Keiji,Totsuka, Yukari,Hada, Noriyasu,Yokoyama, Yuusaku,Suzuki, Hideharu,Mitsunaga, Katsuyoshi

experimental part, p. 455 - 462 (2010/04/29)

9-(4'-Aminophenyl)-9H-pyrido[3,4-b]indole 2 is a mutagenic compound produced by non-mutagenic norharman 1 and aniline in the presence of S9 mix. 9-(4'-Nitrophenyl)-9H-pyrido[3,4-b]indole 4, the relay compound for synthesis of 2, was synthesized starting from ethyl indole-2-aldehyde 12 via initial N-(4-nitro)phenylation of the indole nucleus, elongation of the 2-aldehyde substituent, and then construction of the pyridine nucleus in order to ensure the nitrogen substitution in 2.

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