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103763-87-7

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103763-87-7 Usage

Uses

2-[(2-Aminophenyl)(methyl)amino]ethanol is used as a reactant in the preparation of substituted tetrahydroquinoxalines and tetrahydrobenzo[b][1,4]diazepines by pentamethylcyclopentadienyl iridium-catalyzed hydrogen transfer N-heterocyclization of anilino alcohols.

Check Digit Verification of cas no

The CAS Registry Mumber 103763-87-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,7,6 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 103763-87:
(8*1)+(7*0)+(6*3)+(5*7)+(4*6)+(3*3)+(2*8)+(1*7)=117
117 % 10 = 7
So 103763-87-7 is a valid CAS Registry Number.

103763-87-7SDS

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 2-[2-Amino(methyl)anilino]-1-ethanol

1.2 Other means of identification

Product number -
Other names Ethanamine,2-[[(4-methoxy-2-pyridinyl)methyl]thio]

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:103763-87-7 SDS

103763-87-7Relevant articles and documents

Preparation of substituted 1,2,3,4-tetrahydroquinoxalines and 2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepines from catalytic Cp*Ir hydrogen transfer N-heterocyclization of anilino alcohols

Todd Eary,Clausen, Dane

, p. 6899 - 6902 (2007/10/03)

The [Cp*IrCl2]2/K2CO3 catalyzed hydrogen transfer N-heterocyclization on a series of anilino alcohols has been investigated. The catalyst (20% loading) converts anilino alcohols to 1,2,3,4-tetrahydroquinoxalines and 2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepines in 30-84% isolated yield.

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