Welcome to LookChem.com Sign In|Join Free

CAS

  • or

2270-20-4

2270-20-4

Post Buying Request

2270-20-4 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

2270-20-4 Usage

Chemical Properties

white to off-white crystals or crystalline powder

Uses

5-phenylvaleric acid is used as organic intermediates.

Definition

ChEBI: A monocarboxylic acid that is valeric acid substituted by a phenyl group at the delta-position.

Synthesis Reference(s)

Tetrahedron, 48, p. 9531, 1992 DOI: 10.1016/S0040-4020(01)88320-4

Check Digit Verification of cas no

The CAS Registry Mumber 2270-20-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,7 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2270-20:
(6*2)+(5*2)+(4*7)+(3*0)+(2*2)+(1*0)=54
54 % 10 = 4
So 2270-20-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H14O2/c12-11(13)9-5-4-8-10-6-2-1-3-7-10/h1-3,6-7H,4-5,8-9H2,(H,12,13)/p-1

2270-20-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-phenylpentanoic acid

1.2 Other means of identification

Product number -
Other names EINECS 218-872-8

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:2270-20-4 SDS

2270-20-4Relevant articles and documents

Homoenolic radical derived from propionic acid: A versatile reagent for the radical version of the Michael reaction

Foubelo,Lloret,Yus

, p. 9531 - 9536 (1992)

The homoenolic radical, derived from 3-iodopropionic acid (1) by reaction with in situ generated tributyltin hydride, undergoes clean carbon-carbon forming reaction with electrophilic olefins (2) yielding functionalized acids (3).

-

Anderson,Wang

, p. 277,281 (1954)

-

Carbonylative Transformation of Allylarenes with CO Surrogates: Tunable Synthesis of 4-Arylbutanoic Acids, 2-Arylbutanoic Acids, and 4-Arylbutanals

Wu, Fu-Peng,Li, Da,Peng, Jin-Bao,Wu, Xiao-Feng

supporting information, p. 5699 - 5703 (2019/08/01)

In this Communication, procedures for the selective synthesis of 4-arylbutanoic acids, 2-arylbutanoic acids, and 4-arylbutanals from the same allylbenzenes have been developed. With formic acid or TFBen as the CO surrogate, reactions proceed selectively and effectively under carbon monoxide gas-free conditions.

Strategic Approach to the Metamorphosis of γ-Lactones to NH γ-Lactams via Reductive Cleavage and C-H Amidation

Jung, Hoi-Yun,Chang, Sukbok,Hong, Sungwoo

supporting information, p. 7099 - 7103 (2019/09/07)

A new approach has elaborated on the conversion of γ-lactones to the corresponding NH γ-lactams that can serve as γ-lactone bioisosteres. This approach consists of reductive C-O cleavage and an Ir-catalyzed C-H amidation, offering a powerful synthetic tool for accessing a wide range of valuable NH γ-lactam building blocks starting from γ-lactones. The synthetic utility was further demonstrated by the late-stage transformation of complex bioactive molecules and the asymmetric transformation.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 2270-20-4