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800395-53-3

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800395-53-3 Usage

Compound type

amine

Structure

propan-1-amine backbone with a 4-(tert-butyl)phenyl group attached at the third carbon

Uses

building block for the synthesis of other compounds in chemical and pharmaceutical applications

Handling

must be handled and stored with caution due to potential hazards if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 800395-53-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,0,3,9 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 800395-53:
(8*8)+(7*0)+(6*0)+(5*3)+(4*9)+(3*5)+(2*5)+(1*3)=143
143 % 10 = 3
So 800395-53-3 is a valid CAS Registry Number.

800395-53-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-tert-butylphenyl)propan-1-amine

1.2 Other means of identification

Product number -
Other names 4-tert-Butylphenylpropylamine

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:800395-53-3 SDS

800395-53-3Downstream Products

800395-53-3Relevant articles and documents

Guanidinium and Amidinium Fungicides: A New Class of Crbocation Mimetic Ergosterol Biosynthesis Inhibitors

Arnold, Mary L.,Duriatti, Albert D.,Jung, Michel,Katz, Ruth B.,Liebeschuetz, John W.

, p. 341 - 356 (2007/10/03)

A novel class of chemical has been designed with the aim of inhibiting the Δ14-reductase and Δ8-Δ7-isomerase enzymes in the ergosterol biosynthesis pathway in fungi. Use was made of knowledge about the mechanisms of both e

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