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19492-96-7

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19492-96-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19492-96-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,4,9 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 19492-96:
(7*1)+(6*9)+(5*4)+(4*9)+(3*2)+(2*9)+(1*6)=147
147 % 10 = 7
So 19492-96-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H10OS/c1-2-10(12)9-7-13-11-6-4-3-5-8(9)11/h3-7H,2H2,1H3

19492-96-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1-benzothiophen-3-yl)propan-1-one

1.2 Other means of identification

Product number -
Other names -

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:19492-96-7 SDS

19492-96-7Relevant articles and documents

Synthesis and antidepressant activity of arylalkanol-piperidine derivatives as triple reuptake inhibitors

Zheng, Yong-Yong,Guo, Lin,Zhen, Xue-Chu,Li, Jian-Qi

experimental part, p. 123 - 136 (2012/09/08)

A series of arylalkanol-piperidine derivatives was synthesized, and their triple reuptake inhibition and in vivo activities have been evaluated. Among them, compounds 2a, 2j, 2k, 2m and 2n exhibited high potency for 5-HT, NA and DA transporters. Optimized compounds 2j and 2m showed significant reduction of immobility time compared to that of vehicle in the mouse tail suspension test (TST) test at doses ranging from 10 to 50 mg/kg po, and were not generally motor stimulants at 50 mg/kg dose. In addition, compounds 2j and 2m displayed desirable pharmacokinetic properties in SD rats.

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