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4-(Trimethylsilyl)phenylacetic acid is an organic compound with the chemical formula C11H16O2Si. It is a derivative of phenylacetic acid, where one of the hydrogen atoms on the phenyl ring is replaced by a trimethylsilyl group (Si(CH3)3). This modification enhances the stability and reactivity of the molecule, making it a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. The compound is characterized by its ability to participate in a range of chemical reactions, such as nucleophilic substitutions and electrophilic aromatic substitutions, due to the presence of the electron-donating trimethylsilyl group. It is also known for its applications in protecting groups chemistry, where it can be used to shield reactive sites during complex organic syntheses.

5112-65-2

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5112-65-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5112-65-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,1 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5112-65:
(6*5)+(5*1)+(4*1)+(3*2)+(2*6)+(1*5)=62
62 % 10 = 2
So 5112-65-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H16O2Si/c1-14(2,3)10-6-4-9(5-7-10)8-11(12)13/h4-7H,8H2,1-3H3,(H,12,13)

5112-65-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-trimethylsilylphenyl)acetic acid

1.2 Other means of identification

Product number -
Other names [4-(trimethylsilyl)phenyl]acetic 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:5112-65-2 SDS

5112-65-2Relevant academic research and scientific papers

USE OF T-TYPE CALCIUM CHANNEL BLOCKER FOR TREATING PRURITUS

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, (2022/02/19)

A medicament for treating or preventing pruritus is provided. For the medicament for treating or preventing pruritus, a compound having a blocking action on Cav3.2T-type calcium channels represented by General Formulas (I) to (VI), a tautomer of the compo

T-TYPE CALCIUM CHANNEL BLOCKER

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, (2021/05/29)

To provide a novel T-type calcium channel blocker. A compound represented by the following General Formula (I), a tautomer or a stereoisomer of the compound, a pharmaceutically acceptable salt of the compound, or a solvate of the compound, the tautomer, the stereoisomer, or the salt is used as a T-type calcium channel blocker. wherein A represents a phenyl which may have a substituent, a 4-membered to 6-membered heteroaryl ring composed of one to three identical or different heteroatoms selected from an oxygen atom, a sulfur atom, and a nitrogen atom and carbon atoms as ring-constituting atoms, or a heterocondensed ring composed of the heteroaryl ring and either a benzene ring or a 6-membered heteroaryl ring composed of one to two nitrogen atoms and carbon atoms, wherein the heteroaryl ring or the heterocondensed ring may have a substituent and is bonded to a nitrogen atom of the adjacent cyclic amino by means of a carbon atom constituting these rings; B represents a phenyl which may have a substituent, a 5-membered or 6-membered heteroaryl ring composed of one to three identical or different heteroatoms selected from an oxygen atom, a sulfur atom, and a nitrogen atom and carbon atoms as ring-constituting atoms, or a heterocondensed ring composed of the heteroaryl ring and either a benzene ring or a 6-membered heteroaryl ring composed of one to two nitrogen atoms and carbon atoms, wherein the heteroaryl ring or the heterocondensed ring may have a substituent and is bonded to the adjacent cyclopropyl ring by means of a carbon atom constituting these rings; R1 and R2, which may be identical or different, each represent a hydrogen atom, a halogen atom, or the like; R3 represents a hydrogen atom, a halogen atom, or the like; n and m, which may be identical or different, each represent 0 or 1; and p represents 1 or 2.

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