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6342-77-4

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6342-77-4 Usage

Chemical Properties

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Check Digit Verification of cas no

The CAS Registry Mumber 6342-77-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,4 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6342-77:
(6*6)+(5*3)+(4*4)+(3*2)+(2*7)+(1*7)=94
94 % 10 = 4
So 6342-77-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O3/c1-13-9-5-3-2-4-8(9)6-7-10(11)12/h2-5H,6-7H2,1H3,(H,11,12)/p-1

6342-77-4 Well-known Company Product Price

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  • Alfa Aesar

  • (A14314)  3-(2-Methoxyphenyl)propionic acid, 98+%   

  • 6342-77-4

  • 5g

  • 291.0CNY

  • Detail
  • Alfa Aesar

  • (A14314)  3-(2-Methoxyphenyl)propionic acid, 98+%   

  • 6342-77-4

  • 25g

  • 833.0CNY

  • Detail
  • Alfa Aesar

  • (A14314)  3-(2-Methoxyphenyl)propionic acid, 98+%   

  • 6342-77-4

  • 100g

  • 3038.0CNY

  • Detail

6342-77-4SDS

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-(2-METHOXYPHENYL)PROPIONIC ACID

1.2 Other means of identification

Product number -
Other names 3-(2-methoxyphenyl)propanoic 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:6342-77-4 SDS

6342-77-4Relevant articles and documents

Compounds for and methods of treating diseases

-

, (2021/10/27)

The present invention provides heterocyclic compounds of formula (I) that modulate biological metals and to pharmaceutical compositions containing such compounds. The invention particularly relates to compounds that modulate iron and to compounds for the treatment of diseases, particularly neurological diseases such as Parkinson's disease (PD), Alzheimer's disease (AD), Alzheimer-type dementia, Huntington's disease (HD), amyotrophic lateral sclerosis (ALS), frontotemporal dementia (FTD) and multiple system atrophy (MSA).

Site-Selective, Remote sp3 C?H Carboxylation Enabled by the Merger of Photoredox and Nickel Catalysis

Sahoo, Basudev,Bellotti, Peter,Juliá-Hernández, Francisco,Meng, Qing-Yuan,Crespi, Stefano,K?nig, Burkhard,Martin, Ruben

supporting information, p. 9001 - 9005 (2019/06/24)

A photoinduced carboxylation of alkyl halides with CO2 at remote sp3 C?H sites enabled by the merger of photoredox and Ni catalysis is described. This protocol features a predictable reactivity and site selectivity that can be modulated by the ligand backbone. Preliminary studies reinforce a rationale based on a dynamic displacement of the catalyst throughout the alkyl side chain.

Regioselectivity inversion tuned by iron(iii) salts in palladium-catalyzed carbonylations

Huang, Zijun,Cheng, Yazhe,Chen, Xipeng,Wang, Hui-Fang,Du, Chen-Xia,Li, Yuehui

supporting information, p. 3967 - 3970 (2018/04/23)

Impactful regioselectivity control is crucial for cost-effective chemical synthesis. By using cheap and abundant iron(iii) salts, the hydroxycarbonylations of both aromatic and aliphatic alkenes were significantly enhanced in both reactivity and selectivity (iso/n or n/iso up to >99:1). Moreover, Pd-catalyzed carbonylation selectivity can be switched from branched to linear by using different Fe(iii) salts. In addition, similar results were obtained for the carbonylation of secondary alcohols.

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