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29335-36-2

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29335-36-2 Usage

Uses

Propionamidoxime is used as pharmaceutical intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 29335-36-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,3,3 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 29335-36:
(7*2)+(6*9)+(5*3)+(4*3)+(3*5)+(2*3)+(1*6)=122
122 % 10 = 2
So 29335-36-2 is a valid CAS Registry Number.
InChI:InChI=1/C3H8N2O/c1-2-3(4)5-6/h6H,2H2,1H3,(H2,4,5)

29335-36-2 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
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  • Alfa Aesar

  • (H50889)  Propionamidoxime, 97%   

  • 29335-36-2

  • 250mg

  • 674.0CNY

  • Detail
  • Alfa Aesar

  • (H50889)  Propionamidoxime, 97%   

  • 29335-36-2

  • 1g

  • 2328.0CNY

  • Detail

29335-36-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-hydroxypropanimidamide

1.2 Other means of identification

Product number -
Other names propanamide oxime

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:29335-36-2 SDS

29335-36-2Relevant articles and documents

Process research towards a scalable synthesis of the muscarinic M 1 receptor subtype selective agonist MCD-386

Copp, Richard R.,Abraham, Brent D.,Farnham, James G.,Twose, Trevor M.

, p. 1344 - 1347 (2011)

An efficient process for the M1-selective muscarinic agonist MCD-386 has been developed that offers significant advantages over the original synthetic approach. The new process utilizes an improved preparation of a known symmetrical diamine ester, followed by elaboration to a symmetrical 5-substituted tetrahydropyrimidine. The new route avoids cryogenics and chromatography steps, circumvents an expensive protecting group strategy, and offers significant improvements in cost and throughput.

Discovery and Structure-Activity-Relationship Study of N-Alkyl-5-hydroxypyrimidinone Carboxamides as Novel Antitubercular Agents Targeting Decaprenylphosphoryl-β-D-ribose 2′-Oxidase

Oh, Sangmi,Park, Yumi,Engelhart, Curtis A.,Wallach, Joshua B.,Schnappinger, Dirk,Arora, Kriti,Manikkam, Michelle,Gac, Brian,Wang, Hongwu,Murgolo, Nicholas,Olsen, David B.,Goodwin, Michael,Sutphin, Michelle,Weiner, Danielle M.,Via, Laura E.,Boshoff, Helena I. M.,Barry, Clifton E.

, p. 9952 - 9965 (2018/12/11)

Magnesium plays an important role in infection with Mycobacterium tuberculosis (Mtb) as a signal of the extracellular environment, as a cofactor for many enzymes, and as a structural element in important macromolecules. Raltegravir, an antiretroviral drug

Substituted aminopyrimidine compounds and their method and use thereof

-

Paragraph 1308; 1309, (2017/12/28)

The invention relates to a new aminopyrimidine compound and an application thereof as a drug for treating disorder or diseases related to PI3-kinase abnormity in a free form or a pharmaceutically acceptable salt and preparation form. The invention also relates to a pharmaceutical composition which contains the new aminopyrimidine compound and an application of the pharmaceutical composition in treating mammal disorder or diseases and especially treating human disorder or diseases related to the PI3-kinase abnormity, such as treatment of immunity and inflammatory diseases of PI3-kinase regulation which plays a leading role in a leucocyte function and treatment of proliferative diseases which are related to PI3-kinase activity and include but not limited to leukaemia and solid tumor.

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