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2-Amino-1-benzo[1,3]dioxol-5-yl-ethanol hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40288-57-1

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40288-57-1 Usage

Physical Form

White or off-white crystalline powder

Common Use

Pharmaceutical intermediate

Chemical Structure

A derivative of 1,3-benzodioxole with an amino group and an ethanol moiety attached to the benzene ring

Solubility

Water-soluble due to its hydrochloride salt form

Stability

Stable compound

Applications

Used in the synthesis of various drugs, including antidepressants and antiviral agents.

Check Digit Verification of cas no

The CAS Registry Mumber 40288-57-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,2,8 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 40288-57:
(7*4)+(6*0)+(5*2)+(4*8)+(3*8)+(2*5)+(1*7)=111
111 % 10 = 1
So 40288-57-1 is a valid CAS Registry Number.

40288-57-1SDS

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 2-amino-1-benzo[1,3]dioxol-5-yl-ethanol, hydrochloride

1.2 Other means of identification

Product number -
Other names 2-Amino-1-benzo[1,3]dioxol-5-yl-aethanol, Hydrochlorid

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:40288-57-1 SDS

40288-57-1Downstream Products

40288-57-1Relevant academic research and scientific papers

PROCESS FOR REDUCING BLOOD PRESSURE AND BLOCKING BETA -ADRENERGIC RECEPTOR

-

, (2008/06/13)

Ethanolamine derivatives and their acid addition salts are prepared (1) by reacting a 1-(3,4-methylenedioxyphenyl)-2-aminoethanol compound or an α-amino-(3,4-methylenedioxy)acetophenone compound with an alkanal or an alkanone under reduction conditions, (

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