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35629-70-0

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35629-70-0 Usage

Chemical Properties

Colorless to yellow solid

Synthesis Reference(s)

Journal of Medicinal Chemistry, 14, p. 1075, 1971 DOI: 10.1021/jm00293a014

Check Digit Verification of cas no

The CAS Registry Mumber 35629-70-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,6,2 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 35629-70:
(7*3)+(6*5)+(5*6)+(4*2)+(3*9)+(2*7)+(1*0)=130
130 % 10 = 0
So 35629-70-0 is a valid CAS Registry Number.
InChI:InChI=1/C4H6N2O/c1-3-2-7-4(5)6-3/h2H,1H3,(H2,5,6)

35629-70-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-1,3-oxazol-2-amine

1.2 Other means of identification

Product number -
Other names 4-methyl-oxazole-2-amine

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:35629-70-0 SDS

35629-70-0Relevant articles and documents

Synthesis of 17beta-(2-amino-oxazol-4-yl)-steroids.

Rapi,Ginanneschi,Chelli

, p. 1999 - 2001 (1975)

-

Synthesis and biological evaluation of sulfonamidooxazoles and β-keto sulfones: Selective inhibitors of 11β-hydroxysteroid dehydrogenase type I

Xiang, Jason,Ipek, Manus,Suri, Vipin,Massefski, Walt,Pan, Ning,Ge, Ying,Tam, May,Xing, Yuzhe,Tobin, James F.,Xu, Xin,Tam, Steve

, p. 2865 - 2869 (2007/10/03)

The design, synthesis, and biological evaluation of arylsulfonamidooxazoles as 11β-HSD1 inhibitors and the serendipitous discovery of β-keto sulfones as potent 11β-HSD1 inhibitors are described here. These two classes of compounds are not active against 11β-HSD2 and therefore may have significant therapeutic potential for metabolic syndrome, type 2 diabetes and related metabolic dysfunctions.

Antianaphylactic agents. 1. 2-(Acylamino)oxazoles

Ross,Harrison,Jolley,Neville,Todd,Verge,Dawson,Sweatman

, p. 412 - 417 (2007/10/08)

The synthesis and biological properties of 35 2-(acylamino)oxazoles are described. The majority of the compounds inhibit the release of slow-reacting substance of anaphylaxis (SRS-A) in vitro from sensitized guinea pig chopped lung. In addition, several of the compounds inhibited the release of SRS-A from passively sensitized human chopped lung and protected guinea pigs from the effects of anaphylaxis in a modified Herxheimer test.

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