Welcome to LookChem.com Sign In|Join Free

CAS

  • or

82059-51-6

Post Buying Request

82059-51-6 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

82059-51-6 Usage

Uses

Anxiolytic, autonomic instability.

Check Digit Verification of cas no

The CAS Registry Mumber 82059-51-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,0,5 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 82059-51:
(7*8)+(6*2)+(5*0)+(4*5)+(3*9)+(2*5)+(1*1)=126
126 % 10 = 6
So 82059-51-6 is a valid CAS Registry Number.

82059-51-6SDS

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 (-)-Tofisopam

1.2 Other means of identification

Product number -
Other names (S)-1-(3,4-dimethoxyphenyl)-4-methyl-5-ethyl-7,8-dimethoxy-5H-2,3-benzodiazepine

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:82059-51-6 SDS

82059-51-6Upstream product

82059-51-6Relevant articles and documents

Method of lowering serum uric acid levels with (S)-tofisopam

-

Page/Page column 13, (2016/09/12)

Enantiomerically-pure (S)-tofisopam is administered to lower serum uric acid levels in a mammal.

USE OF TOFISOPAM AS A PDE10A INHIBITOR

-

Page/Page column 16-17, (2008/06/13)

The present invention relates to a novel use of Tofisopam for the preparation of a pharmaceutical composition made for treatment of the positivsymptoms and cognitive deficits in schizophrenic patients.

Method for isolating (R)-tofisopam

-

Page 14, (2008/06/13)

(R)-tofisopam, substantially free of the (S)-enantiomer of tofisopam, is obtained by separating the enantiomers of tofisopam by chromatography employing a chiral separation medium comprising (i) (2S)-2-{(1S)[(3,5-dinitrophenyl)carbonylamino]phenylmethyl}-

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 82059-51-6