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1-Pyrrolidinecarboxylic acid, 2-(1,1-dimethylethoxy)-, phenylmethyl ester, (R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88425-30-3

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88425-30-3 Usage

Molecular structure

1-Pyrrolidinecarboxylic acid, 2-(1,1-dimethylethoxy)-, phenylmethyl ester, (R)-

Type of compound

Nootropic drug

Derivative of

Piracetam

Benefits

Enhances mental performance without causing overstimulation or side effects commonly associated with other stimulant drugs

Popularity

Gaining popularity among individuals seeking to improve cognitive function and focus

Usage

Often used as a study aid or for enhancing productivity.

Check Digit Verification of cas no

The CAS Registry Mumber 88425-30-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,4,2 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 88425-30:
(7*8)+(6*8)+(5*4)+(4*2)+(3*5)+(2*3)+(1*0)=153
153 % 10 = 3
So 88425-30-3 is a valid CAS Registry Number.

88425-30-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(benzyloxycarbonyl)-2-(tert-butyloxy)pyrrolidine

1.2 Other means of identification

Product number -
Other names 2-tert-Butoxy-pyrrolidine-1-carboxylic acid benzyl ester

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:88425-30-3 SDS

88425-30-3Downstream Products

88425-30-3Relevant academic research and scientific papers

Retro-Inverso Isomerization of Peptides: Side Reactions in the Synthesis of N,N'-Diacyl-1,1-diamino-2-phenylethane Derivatives

Chorev, Michael,MacDonald, Scott A.,Goodman, Murray

, p. 821 - 827 (1984)

In general, the synthesis of retro-inverso peptides requires the formation of diacylated gem-diaminoalkyl structures.One way to prepare these gem-diaminoalkyl residues involves the Curtius rearrangement of the N-acylated amino acid hydrazides to the corre

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