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102367-68-0

5-phenyl-1,3,4-thiadiazol-2-amine hydrochloride hydrate is a chemical compound with the molecular formula C9H8ClN3S2.H2O. It is a derivative of 1,3,4-thiadiazol, a heterocyclic compound containing sulfur and nitrogen atoms. 5-phenyl-1,3,4-thiadiazol-2-amine hydrochloride hydrate is characterized by the presence of a phenyl group attached to the 5-position of the thiadiazole ring, and an amine group at the 2-position. The hydrochloride hydrate form indicates that it contains a hydrochloric acid molecule and a water molecule, which are associated with the compound. This chemical is often used in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is important to handle 5-phenyl-1,3,4-thiadiazol-2-amine hydrochloride hydrate with care, as it may have potential health and environmental impacts.

102367-68-0

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102367-68-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102367-68-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,3,6 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 102367-68:
(8*1)+(7*0)+(6*2)+(5*3)+(4*6)+(3*7)+(2*6)+(1*8)=100
100 % 10 = 0
So 102367-68-0 is a valid CAS Registry Number.

102367-68-0SDS

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 5-phenyl-1,3,4-thiadiazol-2-amine,hydrate,hydrochloride

1.2 Other means of identification

Product number -
Other names 1,3,4-Thiadiazole,2-amino-5-phenyl-,hydrochloride,hydrate

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:102367-68-0 SDS

102367-68-0Relevant articles and documents

Unsaturated Compounds containing Nitrogen. Part 5. Reactions of 1,4-Dichloro-1,4-diphenyl-2,3-diazabutadiene with Nucleophiles

Flowers, William T.,Robinson, John F.,Taylor, David R.,Tipping, Anthony E.

, p. 356 - 359 (2007/10/02)

1,4-Dichloro-1,4-diphenyl-2,3-diazabutadiene (1) reacts with potassium cyanate to give 5-phenyl-1,2,4-triazol-3(2H)-one (9), but with potassium thiocyanate it gives the 1-chloro-4-thiocyanato-2,3-diazabutadiene (3).The thiocyanate (3) is not isomerized by heat, but is hydrolysed by acid to a mixture of 2,5-diphenyl-1,3,4-oxadiazole and 2-amino-5-phenyl-1,3,4-thiadiazole.Sodium hydrosulphide, potassium ethylxanthate, and thiourea all convert the dichlorodiazabutadiene (1) into 2,5-diphenyl-1,3,4-thiadiazole, while 2-aminobenzenethiol converts it into 2-phenylbenzothiazole.

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