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1-[(2-methylpropyl)amino]-3-phenoxypropan-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39631-75-9

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39631-75-9 Usage

Type of compound

Amine derivative of propan-2-ol

Structural components

Contains a phenoxy and a methylpropyl group

Potential applications

a. Pharmaceutical ingredient
b. Building block in organic synthesis

Safety considerations

a. Likely to be irritant to eyes
b. Likely to be irritant to skin
c. Likely to be irritant to respiratory system
d. May cause harm to aquatic organisms if released into the environment

Handling precautions

Handle with care, following safety guidelines and regulations

Check Digit Verification of cas no

The CAS Registry Mumber 39631-75-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,6,3 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 39631-75:
(7*3)+(6*9)+(5*6)+(4*3)+(3*1)+(2*7)+(1*5)=139
139 % 10 = 9
So 39631-75-9 is a valid CAS Registry Number.

39631-75-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-methylpropylamino)-3-phenoxypropan-2-ol

1.2 Other means of identification

Product number -
Other names -

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:39631-75-9 SDS

39631-75-9Downstream Products

39631-75-9Relevant academic research and scientific papers

Solvent-Directed Epoxide Opening with Primary Amines for the Synthesis of β-Amino Alcohols

Lizza, Joseph R.,Moura-Letts, Gustavo

, p. 1231 - 1242 (2017)

An efficient synthesis of β-amino alcohols from a variety of epoxides and primary unbranched amines in the absence of any catalyst in high yields and regioselectivities is reported. A variety of polar mixed solvent systems allow for the selective formation of secondary amino alcohols over tertiary amino alcohols. The reaction scope extends to a wide variety of aromatic and aliphatic substituted epoxides and primary amines bearing complex functionality.

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