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4,5,6,7-tetrahydro-1,3-benzoxazol-2-amine is a heterocyclic organic compound with the molecular formula C7H10N2O. It is a derivative of benzoxazole, a five-membered aromatic ring containing oxygen and nitrogen atoms. 4,5,6,7-tetrahydro-1,3-benzoxazol-2-amine is characterized by its unique structure, where the benzene ring is fused with an oxazole ring, and an additional nitrogen atom is present at the 2-position, forming an amine group. It is a colorless solid with potential applications in the synthesis of pharmaceuticals and agrochemicals due to its diverse chemical properties and reactivity. The compound's stability and solubility can vary depending on the specific conditions, and it is often used as an intermediate in the preparation of more complex molecules.

2933-42-8

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2933-42-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2933-42-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,3 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2933-42:
(6*2)+(5*9)+(4*3)+(3*3)+(2*4)+(1*2)=88
88 % 10 = 8
So 2933-42-8 is a valid CAS Registry Number.

2933-42-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5,6,7-tetrahydro-1,3-benzoxazol-2-amine

1.2 Other means of identification

Product number -
Other names 4,5,6,7-Tetrahydro-2-aminobenzoxazole

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:2933-42-8 SDS

2933-42-8Relevant academic research and scientific papers

Discovery and hit-to-lead optimization of novel allosteric glucokinase activators

Lang, Martin,Seifert, Markus H.-J.,Wolf, Kristina K.,Aschenbrenner, Andrea,Baumgartner, Roland,Wieber, Tanja,Trentinaglia, Viola,Blisse, Marcus,Tajima, Nobumitsu,Yamashita, Tokuyuki,Vitt, Daniel,Noda, Hitoshi

, p. 5417 - 5422 (2011/10/12)

We report on a hit generation and hit-to-lead program of a novel class of glucokinase activators (GKAs). Hit compounds, activators at low glucose concentration only were identified by vHTS. Scaffold modification reliably afforded activators also at high s

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