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170151-28-7

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170151-28-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 170151-28-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,1,5 and 1 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 170151-28:
(8*1)+(7*7)+(6*0)+(5*1)+(4*5)+(3*1)+(2*2)+(1*8)=97
97 % 10 = 7
So 170151-28-7 is a valid CAS Registry Number.

170151-28-7SDS

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 (2S)-5,7-difluoro-1,2,3,4-tetrahydronaphthalen-2-amine

1.2 Other means of identification

Product number -
Other names 2-Naphthalenamine,5,7-difluoro-1,2,3,4-tetrahydro-,(2S)

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:170151-28-7 SDS

170151-28-7Downstream Products

170151-28-7Relevant articles and documents

Method for preparing optically pure 5,7-difluoro-1,2,3,4-tetrahydronaphthalene-2-amine and salts thereof

-

, (2021/10/27)

The invention discloses a method for preparing optically pure 5,7-difluoro-1,2,3,4-tetrahydronaphthalene-2-amine as shown in formulas a and b and salts thereof. The method comprises the following steps: (1) reacting 3,5-difluorophenylacetic acid with SOCl2 in the presence of a solvent to generate acyl chloride, and then carrying out Friedel-Crafts reaction on the acyl chloride and ethylene under the action of aluminum trichloride; (2) reacting 5,7-difluoro-3,4-dihydronaphthalene-2(1H)-ketone with amide in an organic solvent under an acid catalysis condition, and performing dehydrating to generate enamine; (3) performing catalytic hydrogenation on enamine in the presence of a chiral catalyst to prepare an optically pure intermediate amide; and (4) hydrolyzing the amide under an acidic or alkaline condition to obtain the optically pure 5,7-difluoro-1,2,3,4-tetrahydronaphthalene-2-amine (a or b) and the form of the salts thereof. The invention provides the method for preparing the optically pure 5,7-difluoro-1,2,3,4-tetrahydronaphthalene-2-amine and salts thereof, which is simple, convenient and easy to industrial production.

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