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79010-42-7

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79010-42-7 Usage

Appearance

Yellowish solid

Molecular weight

136.20 g/mol

Family

Thiadiazole

Substituent

Ethyl

Potential applications

a. Pharmaceutical industry
b. Agrochemical industry

Biological activities

a. Antifungal properties
b. Antibacterial properties

Uses

Building block in the synthesis of various organic compounds

Safety concerns

a. Toxicity
b. Environmental hazards

Handling

Careful handling required due to potential toxicity and environmental hazards

Check Digit Verification of cas no

The CAS Registry Mumber 79010-42-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,0,1 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 79010-42:
(7*7)+(6*9)+(5*0)+(4*1)+(3*0)+(2*4)+(1*2)=117
117 % 10 = 7
So 79010-42-7 is a valid CAS Registry Number.

79010-42-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Amino-5-ethylamino-1,3,4-thiadiazole

1.2 Other means of identification

Product number -
Other names N-ETHYL-1,3,4-THIADIAZOLE-2,5-DIAMINE

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:79010-42-7 SDS

79010-42-7Downstream Products

79010-42-7Relevant articles and documents

Reaction of 4-Alkyl/arylthiosemicarbazides with Cyanamide

Koshy, Lissamma,Joshua, C. P.

, p. 530 - 531 (2007/10/02)

The condensation of cyanamide with 4-alkyl/arylthiosemicarbazide hydrochlorides (I.HCl) results in the formation of 2-alkyl/arylamino-5-amino-1,3,4,-thiadiazoles (III) and 3-amino-4-alkyl/aryl-5-mercapto-1,2,4-triazoles (IV).

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