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N-[(5E)-5-(2-methylbenzylidene)-4-oxo-4,5-dihydro-1,3-thiazol-2-yl]acetamide is a complex organic compound with the molecular formula C12H10N2O2S. It features a 1,3-thiazole ring, which is a five-membered heterocyclic ring containing sulfur and nitrogen atoms. The compound has a 2-yl group attached to the thiazole ring, which is further connected to an acetamide group. The 5-position of the thiazole ring is substituted with a 2-methylbenzylidene group, which is a phenyl ring with a methyl group attached to the 2nd carbon. N-[(5E)-5-(2-methylbenzylidene)-4-oxo-4,5-dihydro-1,3-thiazol-2-yl]acetamide is characterized by a double bond (E configuration) between the 5th and 6th carbon atoms. It is an example of a heterocyclic compound with potential applications in pharmaceuticals or as a chemical intermediate due to its unique structure and reactivity.

5961-39-7

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5961-39-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5961-39-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,6 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5961-39:
(6*5)+(5*9)+(4*6)+(3*1)+(2*3)+(1*9)=117
117 % 10 = 7
So 5961-39-7 is a valid CAS Registry Number.

5961-39-7SDS

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 N-<p-Hydroxy-benzyliden>-2-amino-propan

1.2 Other means of identification

Product number -
Other names N-(p-Hydroxybenzyliden)-isopropylamin

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:5961-39-7 SDS

5961-39-7Relevant academic research and scientific papers

Amaranzole A, a new N-imidazolyl steroid from Phorbas amaranthus

Morinaka, Brandon I.,Masuno, Makoto N.,Pawlik, Joseph R.,Molinski, Tadeusz F.

, p. 5219 - 5222 (2008/09/17)

(Chemical Equation Presented) An unprecedented 24-N-imidazolyl steroidal alkaloid, amaranzole A, was isolated from a tropical sponge, Phorbas amaranthus. The structure was solved by interpretation of MS, NMR, including a novel exciton-coupled CD spectrum

Synthesis and Bleaching Activity of 1,5-Disubstituted Imidazoles

Yamada, Naotaka,Kuwano, Eiichi,Kikuchi, Masamichi,Eto, Morifusa

, p. 1943 - 1948 (2007/10/02)

A variety of 1,5-disubstituted imidazoles and related compounds were prepared, and their bleaching activity was evaluated by using the lettuce seedling test. 5-(4-Benzyloxyphenyl)-1-ethylimidazole (13) caused clear chlorosis, while the 2- and 3-benzyloxyp

Synthesis and Insect Growth Regulatory Activity of 1,5-Disubstituted Imidazoles with Non-terpene Chains

Kuwano, Eiichi,Hisano, Tomomi,Eto, Morifusa

, p. 2999 - 3004 (2007/10/02)

1-Isobutyl-5-(4-phenoxyphenyl)imidazole (KK-98), an inhibitor of juvenile hormone (JH) biosynthesis in the cockroach, and related imidazole compounds were evaluated against silkworm, Bombyx mori, for their activity to induce precocious metamorphosis.KK-98

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