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1,2,5-Thiadiazole-3-carboxaldehyde, 4-methyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90507-36-1

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90507-36-1 Usage

Appearance

Yellow liquid

Molecular weight

147.18 g/mol

Uses

a. Synthesis of pharmaceuticals
b. Synthesis of agrochemicals

Pharmacological and biological activities

Wide range

Potential properties

a. Antioxidant
b. Anticancer

Other reported activities

a. Anti-inflammatory
b. Antimicrobial

Importance

Significant research compound in the field of medicinal chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 90507-36-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,5,0 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 90507-36:
(7*9)+(6*0)+(5*5)+(4*0)+(3*7)+(2*3)+(1*6)=121
121 % 10 = 1
So 90507-36-1 is a valid CAS Registry Number.

90507-36-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-1,2,5-thiadiazole-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 1,2,5-thiadiazole-3-carbaldehyde,4-methyl

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:90507-36-1 SDS

90507-36-1Relevant academic research and scientific papers

Preparation of 1,2,5-Thiadiazole-3-carboxaldehydes

Mataka, Shuntaro,Kurisu, Masayoshi,Takahashi, Kazufumi,Tashiro, Masashi

, p. 325 - 328 (2007/10/02)

1,2,5-Thiadiazole-3-carboxaldehydes 1a-c were prepared by the acid-catalyzed decomposition of 3-azidomethyl-1,2,5-thiadiazoles 2a-c in 68-83percent yields, respectively.Pyrolysis of 2a and 2b afforded the imidazoles 4a and 4b in low yields.NBS-bromination of 1a and 1b gave the corresponding carboxylic acids 10a and 10b via acid bromides 9.Azides 2a and 2b gave the s-triazines 8a and 8b on treatment with NBS.

Nonquaternary cholinesterase reactivators. II. α-Heteroaromatic aldoximes and thiohydroximates as reactivators of ethyl methylphosphonyl-acetylcholinesterase in vitro

Kenley,Bedford,Dailey Jr.,Howd,Miller

, p. 1201 - 1211 (2007/10/02)

We prepared six pairs of α-heteroaromatic aldoximes, RC(=NOH)H, and thiohydroximates, RC(=NOH)S(CH2)2N(C2H5)2, where R represents various oxadiazole and thiadiazole rings. Each compound was characteri

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