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153880-70-7

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153880-70-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 153880-70-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,8,8 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 153880-70:
(8*1)+(7*5)+(6*3)+(5*8)+(4*8)+(3*0)+(2*7)+(1*0)=147
147 % 10 = 7
So 153880-70-7 is a valid CAS Registry Number.

153880-70-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-N-(4-ethoxyphenyl)-N-methylpropanamide

1.2 Other means of identification

Product number -
Other names Propanamide,2-bromo-N-(4-ethoxyphenyl)-N-methyl

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:153880-70-7 SDS

153880-70-7Relevant articles and documents

Racemic N1-norphenserine and its enantiomers: Unpredicted inhibition of human acetyl- and butyrylcholinesterase and β-amyloid precursor protein in vitro

Yu, Qian-Sheng,Luo, Weiming,Holloway, Harold W.,Utsuki, Tada,Perry, Tracy Ann,Lahiri, Debomoy K.,Greig, Nigel H.,Brossi, Arnold

, p. 529 - 539 (2003)

The optically pure enantiomers of N1-norphenserine (15, 16) were synthesized and its racemate 17 was prepared by mixing equal parts of each enantiomer. (-)-N1-Norphenserine (15) was prepared by partial synthesis initiated from the natural product, (-)-physostigmine (1). (+)-N 1-Norphenserine (16) was prepared by total synthesis using the Julian oxindole route, with modifications. The in vitro inhibitory activities of 15-17 were quantified against human erythrocyte AChE and plasma BChE as well as against human neuroblastoma cell β-amyloid precursor protein secretion in cell culture. All were active. Racemic compound (17) with a high AChE and β-amyloid precursor protein inhibitory action may warrant further assessment in Alzheimer's disease models.

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