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Benzenamine, N-ethyl-2,4-dimethoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73674-61-0

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73674-61-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73674-61-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,7 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 73674-61:
(7*7)+(6*3)+(5*6)+(4*7)+(3*4)+(2*6)+(1*1)=150
150 % 10 = 0
So 73674-61-0 is a valid CAS Registry Number.

73674-61-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-ethyl-2,4-dimethoxyaniline

1.2 Other means of identification

Product number -
Other names Benzenamine,N-ethyl-2,4-dimethoxy

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:73674-61-0 SDS

73674-61-0Upstream product

73674-61-0Downstream Products

73674-61-0Relevant academic research and scientific papers

Steric and electronic effects on the reduction of O-silylated aromatic ketoximes with borane

Ortiz-Marciales,Figueroa,Lopez,De Jesus,Vega

, p. 6567 - 6570 (2000)

4-Methoxy acetophenone oximes substituted at the oxygen with TMS, TBS, TIPS and MDPS groups were reduced with borane-THF obtaining the 4-methoxy-N-ethyl aniline as the principal product, up to a 95% yield in the case of the more hindered TIPS group. The 2-methoxy- and 2,4-methoxyacetophenone O-TBS oximes produced only the rearranged secondary aniline. Reduction of 1-indanone O-TBS oximes afforded only the tetrahydroquinoline, whereas the 2-indanone analog provided only 2-aminoindan. (C) 2000 Elsevier Science Ltd.

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