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900158-99-8

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900158-99-8 Usage

General Description

1-(tert-butoxycarbonyl)-5,5-dimethylpyrrolidine-2-carboxylic acid is a chemical compound that belongs to the category of pyrrolidine-2-carboxylic acids. It is composed of a pyrrolidine ring with two methyl groups, a carboxylic acid group, and a tert-butoxycarbonyl (Boc) protecting group attached to the nitrogen atom. 1-(tert-butoxycarbonyl)-5,5-dimethylpyrrolidine-2-carboxylic acid is commonly used in organic synthesis and medicinal chemistry as a protecting group for amines and as a building block for the synthesis of various pharmaceuticals and bioactive molecules. Due to its stability and ease of manipulation, 1-(tert-butoxycarbonyl)-5,5-dimethylpyrrolidine-2-carboxylic acid is a valuable tool in chemical research and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 900158-99-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,0,1,5 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 900158-99:
(8*9)+(7*0)+(6*0)+(5*1)+(4*5)+(3*8)+(2*9)+(1*9)=148
148 % 10 = 8
So 900158-99-8 is a valid CAS Registry Number.

900158-99-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,5-dimethyl-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names -

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:900158-99-8 SDS

900158-99-8Relevant articles and documents

The neuroprotective activity of GPE tripeptide analogues does not correlate with glutamate receptor binding affinity

Alonso De Diego, Sergio A.,Gutierrez-Rodriguez, Marta,Perez de Vega, M. Jesus,Gonzalez-Muniz, Rosario,Herranz, Rosario,Martin-Martinez, Mercedes,Cenarruzabeitia, Edurne,Frechilla, Diana,Rio, Joaquin Del,Jimeno, M. Luisa,Garcia-Lopez, M. Teresa

, p. 3396 - 3400 (2007/10/03)

The influence of several modifications on the GPE tripeptide structure upon the binding to GluRs and on their neuroprotective effects has been studied. The results indicated that the prevention of neuronal death showed by GPE and some analogues is not dir

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