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14150-64-2

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14150-64-2 Usage

Uses

2-Hydrazinylacetic Acid is used as IL-17 and IFN-γ inhibitors for treating autoimmune diseases and chronic inflammation.

Check Digit Verification of cas no

The CAS Registry Mumber 14150-64-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,1,5 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14150-64:
(7*1)+(6*4)+(5*1)+(4*5)+(3*0)+(2*6)+(1*4)=72
72 % 10 = 2
So 14150-64-2 is a valid CAS Registry Number.
InChI:InChI=1/C2H6N2O2/c3-4-1-2(5)6/h4H,1,3H2,(H,5,6)

14150-64-2SDS

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 2-hydrazinylacetic acid

1.2 Other means of identification

Product number -
Other names Hydrazinomethancarbonsaeure

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:14150-64-2 SDS

14150-64-2Relevant articles and documents

Slyusarenko,I.S. et al.

, (1976)

Synthesis method of ethyl hydrazinoacetate hydrochloride

-

Paragraph 0015; 0018; 0021; 0024; 0027; 0030, (2019/01/23)

The invention discloses a synthesis method of ethyl hydrazinoacetate hydrochloride and belongs to the technical field of organic synthesis. The technical scheme is characterized in that chloroacetic acid is used as an initial material to react with hydrazine hydrate to produce intermediate hydrazine acetic acid, hydrazine acetic acid and ethanol form ester to obtain ethyl hydrazinoacetate, a hydrogen chloride solution is added to react to obtain a crude product of ethyl hydrazinoacetate hydrochloride, and high-purity ethyl hydrazinoacetate hydrochloride is obtained through refinement. The method has the advantages of being mild in reaction condition, high in yield, high in purity, low in cost, economical, environmentally friendly, applicable to industrialization and the like and is a synthesis method with industrial production values.

Solution phase synthesis of imidazo[1,2-b]pyrazol-2-one, an interesting 5,5-fused heterocyclic ring system

Blass, Benjamin E.,Srivastava, Anil,Coburn, Keith R.,Faulkner, Amy L.,Janusz, John J.,Ridgeway, James M.,Seibel, William L.

, p. 619 - 621 (2007/10/03)

The solution phase synthesis of a series of imidazo[1,2-b]pyrazol-2-ones, a fused 5,5-ring system, based on diverse set of hydrazino acids and malononitriles is described. The method involves formation of 5-aminopyrazoles followed by intra-molecular cyclodehydration.

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