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380648-94-2

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380648-94-2 Usage

General Description

Tert-butyl (3S,5S)-1-((benzyloxy)carbonyl)-5-(hydroxymethyl)pyrrolidin-3-ylcarbamate is a compound that belongs to the class of carbamates and is composed of tert-butyl, benzyloxy, and pyrrolidin functional groups. It has a pyrrolidine ring structure with a tert-butyl protecting group at the nitrogen and a benzyloxy carbonyl group attached to carbon 1. Additionally, there is a hydroxymethyl group at carbon 5 of the pyrrolidine ring. tert-butyl (3S,5S)-1-((benzyloxy)carbonyl)-5-(hydroxymethyl)pyrrolidin-3-ylcarbamate may have potential applications in medicinal chemistry, drug discovery, or organic synthesis due to its unique structural features and potential biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 380648-94-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,0,6,4 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 380648-94:
(8*3)+(7*8)+(6*0)+(5*6)+(4*4)+(3*8)+(2*9)+(1*4)=172
172 % 10 = 2
So 380648-94-2 is a valid CAS Registry Number.

380648-94-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,4S)-1-benzyloxycarbonyl-4-tert-butoxycarbonylaminopyrrolidine-2-methanol

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

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More Details:380648-94-2 SDS

380648-94-2Relevant articles and documents

Pyrrolidine carbamate nucleic acids: Synthesis and DNA binding studies

Meena,Kumar, Vaijayanti A.

, p. 3393 - 3399 (2007/10/03)

An efficient solid phase synthesis of pyrrolidine carbamate nucleic acids is reported. The protected (2S, 4S)-4-aminopyrrolidine-2-methanol with nucleobases thymine and cytosine attached to the ring nitrogen through an acetyl linker can be activated as ni

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