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128412-15-7

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128412-15-7 Usage

General Description

(3-Bromo-1-methylpropyl)carbamic acid tert-butyl ester is a chemical compound with the molecular formula C8H15BrNO2. It is an ester derivative of a carbamic acid, which is commonly used in organic synthesis and pharmaceutical research. (3-Bromo-1-methylpropyl)carbamic acid tert-butyl ester is often used as a reagent in the production of pharmaceutical drugs and agrochemicals. It is a colorless, odorless liquid that is stable under normal conditions, making it suitable for use in various industrial applications. Additionally, it is important to handle this compound with care, as it may pose health hazards if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 128412-15-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,4,1 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 128412-15:
(8*1)+(7*2)+(6*8)+(5*4)+(4*1)+(3*2)+(2*1)+(1*5)=107
107 % 10 = 7
So 128412-15-7 is a valid CAS Registry Number.

128412-15-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-N-t-butoxycarbonylbutan-3-ylamine

1.2 Other means of identification

Product number -
Other names (3-bromo-1-methyl-propyl)-carbamic 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:128412-15-7 SDS

128412-15-7Downstream Products

128412-15-7Relevant articles and documents

CHK-1 INHIBITORS

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Page/Page column 214, (2010/02/11)

Disclosed are novel inhibitors of Chk-1 and methods of using the same for therapy.

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