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635-51-8

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635-51-8 Usage

Chemical Properties

light beige powder

Synthesis Reference(s)

Synthesis, p. 765, 1986 DOI: 10.1055/s-1986-31770

Check Digit Verification of cas no

The CAS Registry Mumber 635-51-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,3 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 635-51:
(5*6)+(4*3)+(3*5)+(2*5)+(1*1)=68
68 % 10 = 8
So 635-51-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H10O4/c11-9(12)6-8(10(13)14)7-4-2-1-3-5-7/h1-5,8H,6H2,(H,11,12)(H,13,14)/p-2/t8-/m0/s1

635-51-8 Well-known Company Product Price

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  • Alfa Aesar

  • (A11971)  (±)-Phenylsuccinic acid, 98%   

  • 635-51-8

  • 25g

  • 243.0CNY

  • Detail
  • Alfa Aesar

  • (A11971)  (±)-Phenylsuccinic acid, 98%   

  • 635-51-8

  • 100g

  • 663.0CNY

  • Detail
  • Alfa Aesar

  • (A11971)  (±)-Phenylsuccinic acid, 98%   

  • 635-51-8

  • 500g

  • 2699.0CNY

  • Detail

635-51-8SDS

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 DL-Phenylsuccinic acid

1.2 Other means of identification

Product number -
Other names phenylethane-1,2-dicarboxylic 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:635-51-8 SDS

635-51-8Relevant articles and documents

Photoredox Activation of Formate Salts: Hydrocarboxylation of Alkenes via Carboxyl Group Transfer

Huang, Yan,Hou, Jing,Zhan, Le-Wu,Zhang, Qian,Tang, Wan-Ying,Li, Bin-Dong

, p. 15004 - 15012 (2021/12/14)

A photoredox activation mode of formate salts for carboxylation was developed. Using a formate salt as the reductant, carbonyl source, and hydrogen atom transfer reagent, a wide range of alkenes can be converted into acid products via a carboxyl group tra

Harnessing Applied Potential: Selective β-Hydrocarboxylation of Substituted Olefins

Alkayal, Anas,Buckley, Benjamin R.,Malkov, Andrei V.,Montanaro, Stephanie,Tabas, Volodymyr,Wright, Iain A.

supporting information, (2020/02/13)

The construction of carboxylic acid compounds in a selective fashion from low value materials such as alkenes remains a long-standing challenge to synthetic chemists. In particular, β-addition to styrenes is underdeveloped. Herein we report a new electrosynthetic approach to the selective hydrocarboxylation of alkenes that overcomes the limitations of current transition metal and photochemical approaches. The reported method allows unprecedented direct access to carboxylic acids derived from β,β-trisubstituted alkenes, in a highly regioselective manner.

Preparation method and application of tetrahydroisoquinoline derivative

-

Paragraph 0035-0038, (2019/03/08)

The invention discloses a preparation method of a tetrahydroisoquinoline derivative. The tetrahydroisoquinoline derivative is prepared by subjecting 1-(tetrapyrrolidin-1-yl)-1,2,3,4-tetrahydroisoquinoline and 2,3-dihydro-indene-3-one-1-carboxylic acid to condensation. Process conditions are optimized so that preparation steps are simplified. Agents used in the preparation are pollution free. The prepared tetrahydroisoquinoline derivative 1-(tetrapyrrolidin-1-methyl)-2-(2,3-dihydro-indene-3-one-1-carbonyl)-1,2,3,4-tetrahydroisoquinoline can provide good calming effect against neuropathic pain.The tetrahydroisoquinoline derivative has high medical value in drug compositions for pain treatment and in replacing dependent analgesics, such as morphine.

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