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142141-40-0

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142141-40-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 142141-40-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,1,4 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 142141-40:
(8*1)+(7*4)+(6*2)+(5*1)+(4*4)+(3*1)+(2*4)+(1*0)=80
80 % 10 = 0
So 142141-40-0 is a valid CAS Registry Number.

142141-40-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(ethylaminomethyl)aniline

1.2 Other means of identification

Product number -
Other names Ethyl-<2-amino-benzyl>-amin

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:142141-40-0 SDS

142141-40-0Downstream Products

142141-40-0Relevant articles and documents

Regioselective N-alkylation of 2-aminobenzylamine via chelation to 9- BBN

Bar-Haim, Galia,Kol, Moshe

, p. 2643 - 2644 (1998)

A selective synthesis of 2-amino-N-alkylbenzylamines by direct mono alkylation of 2-aminobenzylamine is achieved by a potassium tert- butoxide/alkyl halide treatment of a 9-BBN amine-aminoborane chelate.

Syntheses of 3,4- and 1,4-dihydroquinazolines from 2-aminobenzylamine

Díaz, Jimena E.,Ranieri, Silvia,Gruber, Nadia,Orelli, Liliana R.

supporting information, p. 1470 - 1477 (2017/08/02)

A straightforward strategy for the synthesis of dihydroquinazolines is presented, which allows for the preparation of 3,4- and 1,4-dihydroquinazolines with different substitution patterns from 2-aminobenzylamine (2-ABA) as common precursor. The required functionalization of both amino groups present in 2-ABA was achieved by different routes involving selective N-acylation and cesium carbonate-mediated N-alkylation reactions, avoiding protection/deprotection steps. The heterocycles were efficiently synthesized in short reaction times by microwave-assisted ring closure of the corresponding aminoamides promoted by ethyl polyphosphate (PPE).

NEW COMPOUNDS

-

Page/Page column 22, (2009/01/24)

The present invention encompasses compounds of general Formula (I) wherein R2, R3, Q, W, X, Y and Z are defined as in claim 1, which are suitable for the treatment of diseases characterised by excessive or abnormal cell proliferation

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