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35264-06-3

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35264-06-3 Usage

General Description

(S)-Tert-butoxycarbonylamino-cyclopentyl-acetic acid is a chemical compound that has a molecular formula of C13H21NO4. It is a derivative of acetic acid and contains a cyclopentyl ring. (S)-TERT-BUTOXYCARBONYLAMINO-CYCLOPENTYL-ACETIC ACID is often used as a building block for the synthesis of various pharmaceuticals and biologically active molecules. The tert-butoxycarbonyl (Boc) group is a common protecting group for amines in organic synthesis, and the presence of this group in the compound allows for selective manipulation of the amine functionality. The cyclopentyl group also provides rigidity to the molecule, which can be beneficial for specific applications. Overall, (S)-Tert-butoxycarbonylamino-cyclopentyl-acetic acid is a versatile compound with potential use in drug development and organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 35264-06-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,2,6 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 35264-06:
(7*3)+(6*5)+(5*2)+(4*6)+(3*4)+(2*0)+(1*6)=103
103 % 10 = 3
So 35264-06-3 is a valid CAS Registry Number.

35264-06-3SDS

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 2-cyclopentyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]acetic acid

1.2 Other means of identification

Product number -
Other names 2-cyclopentyl-2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]acetic acid

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:35264-06-3 SDS

35264-06-3Downstream Products

35264-06-3Relevant articles and documents

Straightforward syntheses of furanomycin derivatives and their biological evaluation

Kazmaier, Uli,Paehler, Saskia,Endermann, Rainer,Haebich, Dieter,Kroll, Hein-Peter,Riedl, Bernd

, p. 3905 - 3913 (2002)

Several types of furanomycin analogues were synthesized and investigated with respect to their antibacterial activity. Two different synthetic pathways were developed, based on aldol reactions/ring closing metathesis and an ester enolate Claisen rearrangement. Only the natural product and its desmethyl derivative showed antibacterial activity, pointing towards a narrow structure-activity relationship.

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