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4100-17-8

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4100-17-8 Usage

General Description

1,2,3-Thiadiazole-4-carbonyl chloride is a chemical compound with the molecular formula C2HClN2OS. It is a colorless to light yellow liquid with a pungent odor, and it is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. 1,2,3-Thiadiazole-4-carbonyl chloride (6CI,7CI,8CI,9CI) is an important building block in the preparation of various heterocyclic compounds and is utilized in the pharmaceutical industry for the synthesis of new drug candidates. Additionally, it is also used in the preparation of compounds with potential pesticidal and herbicidal properties. The compound exhibits reactivity as a versatile acylating agent, and it is typically handled and stored under strict safety measures due to its corrosive nature.

Check Digit Verification of cas no

The CAS Registry Mumber 4100-17-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,0 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4100-17:
(6*4)+(5*1)+(4*0)+(3*0)+(2*1)+(1*7)=38
38 % 10 = 8
So 4100-17-8 is a valid CAS Registry Number.

4100-17-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [1,2,3]Thiadiazole-4-carbonyl chloride

1.2 Other means of identification

Product number -
Other names thiadiazole-4-carbonyl chloride

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:4100-17-8 SDS

4100-17-8Relevant articles and documents

Synthesis and antifungal activities of alkyl N-(1,2,3-thiadiazole-4-carbonyl) carbamates and S-alkyl N-(1,2,3-thiadiazole-4-carbonyl) carbamothioates

Li, Zaifeng,Wu, Zengru,Luo, Fuying

, p. 3872 - 3876 (2007/10/03)

A series of alkyl N-(1,2,3-thiadiazole-4-carbonyl) carbamates and S-alkyl N-(1,2,3-thiadiazole-4-carbonyl) carbamothioates with unsubstituted or monobrominated straight chain alkyl groups were synthesized and evaluated as fungistatic agents against Gibberella zeae and Altemaria kikuchiana. These compounds showed variable antifungal activities at concentrations of 5 and 50 μg/mL The results showed that antifungal activities depended on the length of the alkyl chain with the optimal chain length of 6-11 carbons. Carbamic acid, (1,2,3-thiadiazole-4-ylcarbonyl)-, hexyl ester (4) showed a strong fungistatic activity against A. kikuchiana at both concentrations, with 90.7 and 54% growth inhibition at 50 and 5 μg/mL, respectively. Carbamic acid, (1,2,3-thiadiazole-4-ylcarbonyl)-, heptyl ester (5); Carbamic acid, (1,2,3-thiadiazole-4-ylcarbonyl)-, octyl ester (6); and Carbamic acid, (1,2,3-thiadiazole-4-ylcarbonyl)-, undecyl ester (9) showed strong fungistatic activity against G. zeae at both concentrations. Their growth inhibitions against G. zeae at the concentration of 5 μg/mL were 78, 63, and 59%, respectively.

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