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74834-46-1

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74834-46-1 Usage

Uses

thiazolidin e thione pharmaceutical intermediate

Check Digit Verification of cas no

The CAS Registry Mumber 74834-46-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,8,3 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 74834-46:
(7*7)+(6*4)+(5*8)+(4*3)+(3*4)+(2*4)+(1*6)=151
151 % 10 = 1
So 74834-46-1 is a valid CAS Registry Number.

74834-46-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-bromobenzoyl)-1,3-thiazolidine-2-thione

1.2 Other means of identification

Product number -
Other names 3-(p-bromobenzoyl)-1,3-thiazolidine-2-thione

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:74834-46-1 SDS

74834-46-1Downstream Products

74834-46-1Relevant articles and documents

3-(P-BROMOBENZOYL)-1,3-THIAZOLIDINE-2-THIONE

Bryan, R. F.,Hartley, P.,Peckler, S.,Fujita, E.,Nagao, Y.,Seno, K.

, p. 1709 - 1710 (1980)

C10H8BrNOS2, orthorombic, Pbca, a = 7.166 (4), b = 14.716 (9), c = 21.507 (12) Angstroem (λ = 1.5418 Angstroem), U = 2268 Angstroem3, Z = 8, Dx = 1.77 Mg m-3 = Dm (flotation in C2H5I/toluene), F(000) = 1200, μ(C

Utilisation of Sulphur-containing Leaving Groups. Part 2. Monitored Reduction of Carboxylic Acids into Alcohols or Aldehydes via 3-Acylthiazolidine-2-thiones by Sodium Borohydride or Di-isobutylaluminium Hydride

Nagao, Yoshimitsu,Kawabata, Kohji,Seno, Kaoru,Fujita, Eiichi

, p. 2470 - 2473 (2007/10/02)

3-Acylthiazolidine-2-thiones (2) have been prepared by three methods, and treated with di-isobutylaluminium hydride or sodium borohydride to give aldehyde or alcohol in high yield, respectively.The original yellow colour disappears when reduction is finished, enabling the reaction to be monitored.The high reactivity of the carbonyl group in amide (2) was briefly discussed.

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