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(+)-(1R)-4-methyl-cyclohex-3-enecarboxylic acid is a carboxylic acid compound with an optically active (1R) configuration, featuring a cyclohexene ring with a carboxylic acid group and a methyl group at the fourth position. This unique structure and properties make it a valuable building block in organic synthesis and medicinal chemistry for the development of pharmaceuticals and biologically active compounds.

121424-36-0

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121424-36-0 Usage

Uses

Used in Pharmaceutical Industry:
(+)-(1R)-4-methyl-cyclohex-3-enecarboxylic acid is used as a building block for the synthesis of various pharmaceuticals and biologically active compounds due to its unique structure and properties.
Used in Organic Synthesis:
(+)-(1R)-4-methyl-cyclohex-3-enecarboxylic acid is used as a key intermediate in the synthesis of complex organic molecules, contributing to the development of new drugs and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 121424-36-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,4,2 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 121424-36:
(8*1)+(7*2)+(6*1)+(5*4)+(4*2)+(3*4)+(2*3)+(1*6)=80
80 % 10 = 0
So 121424-36-0 is a valid CAS Registry Number.

121424-36-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-(1R)-4-methyl-cyclohex-3-enecarboxylic acid

1.2 Other means of identification

Product number -
Other names .(R)-4-methylcyclohex-3-ene carboxylic 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:121424-36-0 SDS

121424-36-0Relevant articles and documents

Silent catalytic promiscuity in the high-fidelity terpene cyclase δ-cadinene synthase

Loizzi, Marianna,Miller, David J.,Allemann, Rudolf K.

, p. 1206 - 1214 (2019/02/07)

δ-Cadinene synthase (DCS) is a high-fidelity sesquiterpene synthase that generates δ-cadinene as the sole detectable organic product from its natural substrate (E,E)-FDP. Previous work with this enzyme using substrate analogues revealed the ability of DCS

Synthesis of a Chiral Auxiliary Family from Levoglucosenone and Evaluation in the Diels-Alder Reaction

Klepp, Julian,Sumby, Christopher J.,Greatrex, Ben W.

supporting information, p. 1441 - 1446 (2018/06/08)

A new family of chiral auxiliaries has been developed based on the lignocellulosic biomass pyrolysis product levoglucosenone. A promising single stereoisomer with an alcohol and π-stacking phenyl substituents was prepared in excellent yield in two steps from dihydrolevoglucosenone without chromatography on >50 g scale. Acrylate esters prepared from the auxiliaries underwent diastereoselective Lewis acid promoted Diels-Alder reactions with cyclopentadiene (endo / exo 98:2, endo d. r. up to 98:2), dimethylbutadiene (d.r. 93:7), and isoprene (d.r. > 98:2).

SOLID FORMS OF 2-(TERT-BUTYLAMINO)-4-((1R,3R,4R)-3-HYDROXY-4-METHYLCYCLOHEXYLAMINO)-PYRIMIDINE-5-CARBOXAMIDE, COMPOSITIONS THEREOF AND METHODS OF THEIR USE

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Paragraph 0651; 0652, (2015/08/04)

Provided herein are formulations, processes, solid forms and methods of use relating to 2-(tert-butylamino)-4-((1R,3R,4R)-3-hydroxy-4-methylcyclohexylamino)-pyrimidine-5-carboxamide.

SOLID FORMS OF 2-(TERT-BUTYLAMINO)-4-((1R,3R,4R)-3-HYDROXY-4-METHYLCYCLOHEXYLAMINO)-PYRIMIDINE-5-CARBOXAMIDE, COMPOSITIONS THEREOF AND METHODS OF THEIR USE

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Paragraph 00453, (2015/11/02)

Provided herein are formulations, processes, solid forms and methods of use relating to 2- (tert-butylamino)-4-((lR,3R,4R)-3-hydroxy-4-methylcyclohexylamino)-pyrimidine-5- carboxamide.

SYNTHESIS OF AN ANTIVIRAL COMPOUND

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Paragraph 0188; 0189, (2014/03/22)

The present disclosure provides processes for the preparation of a compound of Formula I: which is useful as an antiviral agent. The disclosure also provides compounds that are synthetic intermediates to compounds of formula.

SYNTHESIS OF AN ANTIVIRAL COMPOUND

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Paragraph 0139, (2014/03/22)

The present disclosure provides a processes for the preparation of a compound of Formula I: which is useful as an antiviral agent. The disclosure also provides compounds that are synthetic intermediates to compounds of Formula I.

METHODS FOR TREATING HCV

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Page/Page column 81-82, (2013/03/28)

This invention relates to combinations of therapeutic molecules useful for treating hepatitis C virus infection. The present invention relates to methods, uses, dosing regimens, and compositions.

METHODS FOR TREATING HCV

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Paragraph 0324, (2013/10/22)

This invention relates to combinations of therapeutic molecules useful for treating hepatitis C virus infection. The present invention relates to methods, uses, dosing regimens, and compositions.

THIOPHEN-2-CARBOXYLIC ACID DERIVATIVES USEFUL AS INHIBITORS OF FLAVIVIRIDAE VIRUSES

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Page/Page column 35; 36; 38, (2013/03/26)

Provided are compounds of Formula I: and pharmaceutically acceptable salts and esters thereof. The compounds, compositions, and methods provided are useful for the treatment of Flaviviridae virus infections (e.g. hepatitis C infections), particularly drug

Second generation levoglucosenone-derived chiral auxiliaries. Scope and application in asymmetric Diels-Alder reactions

Sarotti, Ariel M.,Spanevello, Rolando A.,Suárez, Alejandra G.

supporting information; experimental part, p. 3502 - 3508 (2009/08/15)

Chiral alcohols were designed and easily prepared from levoglucosenone, a biomass-derived valuable synthon. These alcohols were tested as chiral auxiliaries in asymmetric Diels-Alder reactions between the corresponding acrylates with acyclic and cyclic di

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