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886366-16-1

1-(3-METHYLPHENYL)CYCLOPROPANECARBOXYLIC ACID is an organic compound derived from (3-METHYLPHENYL)ACETONITRILE (M288715). It is characterized by a cyclopropane ring fused with a carboxylic acid group and a 3-methylphenyl moiety. This unique structure endows it with potential applications in the pharmaceutical industry.

886366-16-1

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886366-16-1 Usage

Uses

Used in Pharmaceutical Industry:
1-(3-METHYLPHENYL)CYCLOPROPANECARBOXYLIC ACID is used as a reactant for synthesizing potential non-nucleoside reverse transcriptase inhibitors (NNRTIs) for the treatment of HIV. Its unique structure allows it to inhibit the replication of the virus, offering a potential therapeutic option for HIV-infected individuals.
Additionally, 1-(3-METHYLPHENYL)CYCLOPROPANECARBOXYLIC ACID is used as a reactant to prepare hepatitis C virus inhibitors. Its ability to target specific viral enzymes or pathways makes it a valuable component in the development of antiviral medications, potentially leading to more effective treatments for hepatitis C.

Check Digit Verification of cas no

The CAS Registry Mumber 886366-16-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,3,6 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 886366-16:
(8*8)+(7*8)+(6*6)+(5*3)+(4*6)+(3*6)+(2*1)+(1*6)=221
221 % 10 = 1
So 886366-16-1 is a valid CAS Registry Number.

886366-16-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-methylphenyl)cyclopropane-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names -

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:886366-16-1 SDS

886366-16-1Downstream Products

886366-16-1Relevant articles and documents

Chiral Bidentate Boryl Ligand Enabled Iridium-Catalyzed Enantioselective C(sp3)-H Borylation of Cyclopropanes

Shi, Yongjia,Gao, Qian,Xu, Senmiao

supporting information, p. 10599 - 10604 (2019/08/28)

We herein report an Ir-catalyzed enantioselective C(sp3)-H borylation of cyclopropanecarboxamides using a chiral bidentate boryl ligand for the first time. A variety of substrates with α-quaternary carbon centers could be compatible in this reaction to provide β-borylated products with good to excellent enantioselectivities. We have also demonstrated that the borylated products can be used as versatile precursors engaging in stereospecific transformations of C-B bonds, including the synthesis of a bioactive compound Levomilnacipran.

Rhodium-Catalyzed Enantioselective Silylation of Cyclopropyl C?H Bonds

Lee, Taegyo,Hartwig, John F.

supporting information, p. 8723 - 8727 (2016/07/21)

Hydrosilyl ethers, generated in situ by the dehydrogenative silylation of cyclopropylmethanols with diethylsilane, undergo asymmetric, intramolecular silylation of cyclopropyl C?H bonds in high yields and with high enantiomeric excesses in the presence of

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