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95388-79-7

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95388-79-7 Usage

Description

Tert-Butyl 4-chlorobutylcarbamate, also known as tBoc-4-chlorobutylcarbamate, is a chemical compound that serves as a protecting group in organic synthesis. It is synthesized from tert-butyl isocyanate and 4-chlorobutan-1-ol and is particularly noted for its role in the pharmaceutical industry where it is utilized to shield amine functional groups from undesired reactions during chemical synthesis. Its ease of removal under mild conditions makes it a favored choice for protecting amine groups in peptide synthesis. Furthermore, it finds applications in the manufacturing of specialty chemicals and agrochemicals. As with all chemical compounds, it is imperative to exercise proper safety measures during its handling and use.

Uses

Used in Pharmaceutical Industry:
Tert-Butyl 4-chlorobutylcarbamate is used as a protecting group for amine functional groups during chemical synthesis, ensuring that these groups remain intact and unreacted until the protective group is intentionally removed. This selective protection is crucial for the successful synthesis of complex pharmaceutical compounds.
Used in Peptide Synthesis:
In the field of peptide synthesis, tert-Butyl 4-chlorobutylcarbamate is employed as a protecting agent for amine groups. Its easy removal under mild conditions allows for the controlled deprotection of amine groups at specific stages of the synthesis process, facilitating the stepwise assembly of peptide chains.
Used in Specialty Chemicals Production:
Tert-Butyl 4-chlorobutylcarbamate is utilized in the production of specialty chemicals, where its protective properties are harnessed to control the reactivity of amine groups during the synthesis of various chemical products.
Used in Agrochemicals Production:
Similarly, in the agrochemicals industry, tert-Butyl 4-chlorobutylcarbamate is used to protect amine groups during the synthesis of active ingredients for pesticides and other agricultural chemicals, ensuring the successful creation of desired products with specific biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 95388-79-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,3,8 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 95388-79:
(7*9)+(6*5)+(5*3)+(4*8)+(3*8)+(2*7)+(1*9)=187
187 % 10 = 7
So 95388-79-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H18ClNO2/c1-9(2,3)13-8(12)11-7-5-4-6-10/h4-7H2,1-3H3,(H,11,12)

95388-79-7SDS

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 tert-butyl N-(4-chlorobutyl)carbamate

1.2 Other means of identification

Product number -
Other names TERT-BUTYL 4-CHLOROBUTYLCARBAMATE

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:95388-79-7 SDS

95388-79-7Downstream Products

95388-79-7Relevant articles and documents

DECONSTRUCTIVE FUNCTIONALIZATION METHODS AND COMPOUNDS

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Paragraph 0464-0467, (2020/01/31)

Disclosed herein, inter alia, are deconstructive functionalization methods and compounds made using the same.

ORGANIC COMPOUNDS

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Page/Page column 134, (2008/06/13)

A compound of formula (I) or tautomers, or stereoisomers, or solvates, or pharmaceutically acceptable salts thereof, wherein M1, M1, L1, L2, W1, W2, X1, X2, Y1, Y2, A, R5 and R5a are as defined herein for the for treatment of conditions mediated by the blockade of an epithelial sodium channel, particularly an inflammatory or allergic condition.

Malonic acid derivatives and methods for their synthesis

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, (2008/06/13)

The present invention refers to a new class of malonic acid derivatives of general formula I STR1 wherein R1 and R2, each independently, represent hydrogen or a carboxyl protecting group, and the residue R corresponds to the side-cha

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