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25860-44-0

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25860-44-0 Usage

General Description

2-Phenyl-pyrrolidine-2-carboxylic acid is a chemical compound which belongs to the class of compounds known as phenylpyrrolidines. As suggested by its name, the structure of the compound includes a pyrrolidine ring, a type of cyclic secondary amine, linked to a phenyl group and a carboxylic acid group. 2-PHENYL-PYRROLIDINE-2-CARBOXYLIC ACID may have a variety of applications in pharmaceutical and material science due to its combination of functional groups. However, as with all chemicals, it needs to be handled with care as it may pose potential risks and hazards, such as possible irritation to eyes, skin, and respiratory system. Its reactivity, stability, and possible toxicological properties need to be studied in detail for potential industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 25860-44-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,8,6 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 25860-44:
(7*2)+(6*5)+(5*8)+(4*6)+(3*0)+(2*4)+(1*4)=120
120 % 10 = 0
So 25860-44-0 is a valid CAS Registry Number.

25860-44-0SDS

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 2-phenylpyrrolidine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names HMS1697M21

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:25860-44-0 SDS

25860-44-0Relevant articles and documents

A new sparteine surrogate for asymmetric deprotonation of N-Boc pyrrolidine

Stead, Darren,O'Brien, Peter,Sanderson, Adam

supporting information; experimental part, p. 1409 - 1412 (2009/04/12)

(Chemical Equation Presented) The s-BuLi complex of a cyclohexane-derived diamine is as efficient as s-BuLi/(-)-sparteine for the asymmetric deprotonation of N-Boc pyrrolidine. This is the first example of high enantioselectivity using a non-sparteine-like diamine in such reactions. The ( S, S)-diamine is a useful (+)-sparteine surrogate and was utilized in short syntheses of (-)-indolizidine 167B and an intermediate for the synthesis of the CCK antagonist (+)-RP 66803.

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