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135066-21-6

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135066-21-6 Usage

General Description

4-tert-Butoxyphenylacetic acid is a chemical compound with a molecular formula C12H16O3. It is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. 4-TERT-BUTOXYPHENYLACETIC ACID is a derivative of phenylacetic acid and contains a tert-butoxy group attached to the phenyl ring. It is a white crystalline solid with a melting point of 79-83°C. This chemical is known for its potential therapeutic effects, including anti-inflammatory and analgesic properties, and is used in the manufacturing of medications for pain relief and anti-inflammatory treatments. Additionally, it has been studied for its potential as an inhibitor of fatty acid amide hydrolase, an enzyme involved in the regulation of endocannabinoid signaling. Overall, 4-tert-butoxyphenylacetic acid is a versatile compound with various potential applications in the pharmaceutical and agricultural industries.

Check Digit Verification of cas no

The CAS Registry Mumber 135066-21-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,0,6 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 135066-21:
(8*1)+(7*3)+(6*5)+(5*0)+(4*6)+(3*6)+(2*2)+(1*1)=106
106 % 10 = 6
So 135066-21-6 is a valid CAS Registry Number.

135066-21-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[4-[(2-methylpropan-2-yl)oxy]phenyl]acetic acid

1.2 Other means of identification

Product number -
Other names 4-tert-Butoxyphenylacetic 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:135066-21-6 SDS

135066-21-6Relevant articles and documents

A novel constrained reduced-amide inhibitor of HIV-1 protease derived from the sequential incorporation of γ-turn mimetics into a model substrate

Newlander,Callahan,Moore,Tomaszek Jr.,Huffman

, p. 2321 - 2331 (2007/10/02)

C7 mimetics, designed to lock three amino acid residues of a peptide chain into a γ-turn conformation, were introduced sequentially between the P3 to P2' positions of a model HIV-1 protease substrate I (resulting in compou

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