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42288-08-4

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42288-08-4 Usage

General Description

3-METHYL-3-(4-METHYLPHENYL)BUTANOIC ACID is a chemical compound with the molecular formula C13H18O2. It is a derivative of butanoic acid and has the systematic name 3-methyl-3-(4-methylphenyl)butanoic acid. It is a white crystalline solid that is commonly used in the pharmaceutical industry as a building block for the synthesis of various drugs and pharmaceutical compounds. 3-METHYL-3-(4-METHYLPHENYL)BUTANOIC ACID is known for its anti-inflammatory and analgesic properties and is often used in the development of non-steroidal anti-inflammatory drugs (NSAIDs). Additionally, it has also been studied for its potential use in the treatment of chronic pain and inflammatory conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 42288-08-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,2,8 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 42288-08:
(7*4)+(6*2)+(5*2)+(4*8)+(3*8)+(2*0)+(1*8)=114
114 % 10 = 4
So 42288-08-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H16O2/c1-9-4-6-10(7-5-9)12(2,3)8-11(13)14/h4-7H,8H2,1-3H3,(H,13,14)

42288-08-4SDS

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 3-METHYL-3-(4-METHYLPHENYL)BUTANOIC ACID

1.2 Other means of identification

Product number -
Other names 3-Methyl-3-p-tolyl-buttersaeure

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:42288-08-4 SDS

42288-08-4Relevant articles and documents

Photocatalytic Neophyl Rearrangement and Reduction of Distal Carbon Radicals by Iminyl Radical-Mediated C?C Bond Cleavage

Yu, Xiao-Ye,Wang, Peng-Zi,Yan, Dong-Mei,Lu, Bin,Chen, Jia-Rong,Xiao, Wen-Jing

, p. 3601 - 3606 (2018/09/18)

The control of selectivity in the reactions of the highly reactive open-shell carbon radicals is an attractive but often challenging task. Building on the strategy of photoinduced iminyl radical-mediated C?C bond cleavage, we have developed photocatalytic neophyl rearrangement and reduction of distal carbon radicals under visible light irradiation of O-acyl oximes. This mild protocol tolerates a wide range of readily available O-acyl oximes, enabling facile synthesis of diversely substituted α,β-unsaturated nitriles and β-functionalized saturated nitriles in a highly selective manner. (Figure presented.).

Non-peptide compounds affecting the action of gonadotropin-releasing hormone (GnRH)

-

, (2008/06/13)

Non-peptide GnRH agents that inhibit the effect of gonadotropin-releasing hormone are described. Such agents are useful for treating mammalian reproductive disorders and steroid hormone-dependent tumors as well as for regulating fertility, where suppressi

Steric Effects. A Study of a Rationally Designed System

Bott, Garry,Field, Leslie D.,Sternhell, Sever

, p. 5618 - 5626 (2007/10/02)

The principles for the rational design of systems suitable for the study of steric effects are defined.A suitable molecular framework was synthesized and a study of internal rotaition by dynamic NMR spectroscopy (DNMR) 0f 33 derivatives, differing principally in the nature of the molecular fragment (X), showed the following. (i) For 1 (Y = Me; X = halogen) the rotaition barriers (ΔG excit.) increase smoothly and monotonically with the van der Waals radius of X (rx), which permits the estimation of effective rx for fragments of lower symmetry. (ii) The rotational barriers are the sum of additive contributions, designated interference values (IH-X), which can be used to predict the rotational barriers in 2,2'-disubstituted biphenyls. (iii) A simple geometrical parameter, apparent overlap (r*), which is related to the distortion of the framework in the transition state, is proposed and found to have an excellent linear correlation with the barrier to rotation in 2,2'-disubstituted biphenyls. (iv) This correlation can be used for a semiquantitative estimation of rotational barriers in biaryls and other systems.

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