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64958-77-6

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64958-77-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64958-77-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,9,5 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 64958-77:
(7*6)+(6*4)+(5*9)+(4*5)+(3*8)+(2*7)+(1*7)=176
176 % 10 = 6
So 64958-77-6 is a valid CAS Registry Number.

64958-77-6SDS

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 2,4-dimethyl-3-N,5-N-bis(4-methylphenyl)-1,2,4-thiadiazolidine-3,5-diimine

1.2 Other means of identification

Product number -
Other names 1,2,4-Thiadiazolidine,benzenamine deriv.

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:64958-77-6 SDS

64958-77-6Downstream Products

64958-77-6Relevant articles and documents

Selective oxidation of thioureas in an ionic liquid by employing an ion-supported hypervalent iodine(III) reagent

Qian, Weixing,Jin, Erlei,Bao, Weiliang,Zhang, Yongmin

, p. 613 - 616 (2007/10/03)

Several 2,4-dialkyl-3,5-bis(arylimino)-1,2,4-thiadiazolidines were synthesised under mild conditions in good yield by the selective oxidation of N-alkyl-N′-arylthioureas by using 1-(4-diacetoxyiodobenzyl)-3-methyl imidazolium tetrafluoroborate [dibmim]su

'Synthesis, antiinflammatory and analgesic activities of some 1,2,4-thiadiazolidines and 1-4-aryl guanidines'

Naik,Pandeya

, p. 289 - 293 (2007/10/02)

A series of 2,4-dimethyl-3,5-diarylimino-1,2,4-thiadiazolidines (1a-1) and 1-[2-(substituted benzothiazolyl]-1,3-dimethyl-4-aryl guanidines (2a-1) were evaluated for their anti-inflammatory and analgesic activities. Substitution of p-methoxy group (1c and

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