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10276-09-2

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10276-09-2 Usage

Uses

2,2-Dimethyl-3-butenoic Acid is an constituent in the synthesis of metabolites of Simvastatin (S485000), a synthetic derivative of a fermentation product of Aspergillus terreus.

Synthesis Reference(s)

The Journal of Organic Chemistry, 34, p. 1717, 1969 DOI: 10.1021/jo01258a041

Check Digit Verification of cas no

The CAS Registry Mumber 10276-09-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,7 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10276-09:
(7*1)+(6*0)+(5*2)+(4*7)+(3*6)+(2*0)+(1*9)=72
72 % 10 = 2
So 10276-09-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O2/c1-4-6(2,3)5(7)8/h4H,1H2,2-3H3,(H,7,8)

10276-09-2 Well-known Company Product Price

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  • Alfa Aesar

  • (H64067)  2,2-Dimethyl-3-butenoic acid, 95%   

  • 10276-09-2

  • 250mg

  • 343.0CNY

  • Detail
  • Alfa Aesar

  • (H64067)  2,2-Dimethyl-3-butenoic acid, 95%   

  • 10276-09-2

  • 1g

  • 1029.0CNY

  • Detail
  • Alfa Aesar

  • (H64067)  2,2-Dimethyl-3-butenoic acid, 95%   

  • 10276-09-2

  • 5g

  • 4116.0CNY

  • Detail

10276-09-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-Dimethylbut-3-enoic acid

1.2 Other means of identification

Product number -
Other names 2,2-dimethylbut-3-enoic acid

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:10276-09-2 SDS

10276-09-2Relevant articles and documents

An oxidative approach to a hydroxypiperidinone utilizing a Rh-catalyzed C-H activation process

Ayers, Timothy A.

, p. 1415 - 1418 (2013)

C-H activation and isomerization using a Rh-catalyst provided quick access to dehydropiperidine derivatives that could be further oxidized to hydroxypiperidinone derivatives.

Caesium fluoride-mediated hydrocarboxylation of alkenes and allenes: Scope and mechanistic insights

Gevorgyan, Ashot,Obst, Marc F.,Guttormsen, Yngve,Maseras, Feliu,Hopmann, Kathrin H.,Bayer, Annette

, p. 10072 - 10078 (2019/11/14)

A caesium fluoride-mediated hydrocarboxylation of olefins is disclosed that does not rely on precious transition metal catalysts and ligands. The reaction occurs at atmospheric pressures of CO2 in the presence of 9-BBN as a stoichiometric reductant. Stilbenes, β-substituted styrenes and allenes could be carboxylated in good yields. The developed methodology can be used for preparation of commercial drugs as well as for gram scale hydrocarboxylation. Computational studies indicate that the reaction occurs via formation of an organocaesium intermediate.

KINASE INHIBITORS AND USES THEREOF

-

Paragraph 0256; 0342, (2018/12/13)

The present disclosure relates generally to compounds and compositions, intermediates, processes for their preparation, and their use as kinase inhibitors.

COMBINATIONS OF HEPATITIS C VIRUS INHIBITORS

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Page/Page column 722; 723, (2015/02/02)

The present disclosure is generally directed to antiviral compounds, and more specifically directed to combinations of compounds which can inhibit the function of the NS5A protein encoded by Hepatitis C virus (HCV), compositions comprising such combinations, and methods for inhibiting the function of the NS5A protein.

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