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63984-03-2

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63984-03-2 Usage

General Description

Tert-butyl 5-aminopentanoate is a chemical compound consisting of a 5-aminopentanoate group attached to a tert-butyl group. It is commonly used in organic synthesis, particularly as a reagent for the preparation of various pharmaceuticals and other biologically active compounds. It has been found to exhibit antimicrobial and antifungal properties, making it useful in the development of new drugs and treatments. Additionally, tert-butyl 5-aminopentanoate is known for its low toxicity and relatively stable nature, making it a safe and versatile chemical for use in research and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 63984-03-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,9,8 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 63984-03:
(7*6)+(6*3)+(5*9)+(4*8)+(3*4)+(2*0)+(1*3)=152
152 % 10 = 2
So 63984-03-2 is a valid CAS Registry Number.

63984-03-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name δ-aminovaleric acid tert-butyl ester

1.2 Other means of identification

Product number -
Other names 5-aminovaleric acid tert.-butyl 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:63984-03-2 SDS

63984-03-2Relevant articles and documents

SUBSTITUTED 2,3-BENZODIAZEPINES DERIVATIVES

-

, (2021/08/06)

Derivatives of 2,3- benzodiazepines as inhibitors of Bromodomain and extra C-terminal domain (BET) proteins, in particular the BRD4 family member, methods of preparing said compounds, intermediate compounds useful for preparing said compounds, pharmaceuti

Heterovalent inhibitors targeting N-end Rule Pathway and its use

-

, (2016/10/10)

An alkali-soluble polymer resin compound of formula 1 a including N-end Rule pathway inhibitors disclosure the composition. According to type 1 and type 2 herein each compounds recognizing substrate UBR box and a ClpS box a mammal having two tolerance N-e

Building Units for N-Backbone Cyclic Peptides. 3. Synthesis of Protected Nα-(ω-Aminoalkyl)amino Acids and Nα-(ω-Carboxyalkyl)amino Acids

Muller, Dan,Zeltser, Irena,Bitan, Gal,Gilon, Chaim

, p. 411 - 416 (2007/10/03)

An improved synthesis of a family of amino acids that contain ω-aminoalkyl groups and of a new family containing ω-carboxyalkyl groups linked to the α-amine is described. The synthesis was performed by alkylation of suitably monoprotected alkylenediamines and protected ω-amino acids with triflates of α-hydroxy acid esters. The reaction proceeded with inversion of configuration yielding optically pure products. The Nα-(ω-aminoalkyl)amino acids and Nα-(ω-carboxyalkyl)amino acids were orthogonally protected to allow their incorporation into peptides by solid-phase peptide synthesis (SPPS) methodology.

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