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35970-31-1

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35970-31-1 Usage

Also known as

6-Amino-2,3-dihydro-2,3-dioxo-1,3-benzodioxol-5-ol
Used in the pharmaceutical industry as a building block for the synthesis of various drugs and drug candidates
Potential therapeutic applications in the treatment of conditions such as cancer, inflammation, and infectious diseases
Used in research laboratories for the development of new pharmaceutical compounds
Used as a tool for studying biological processes

Check Digit Verification of cas no

The CAS Registry Mumber 35970-31-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,9,7 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 35970-31:
(7*3)+(6*5)+(5*9)+(4*7)+(3*0)+(2*3)+(1*1)=131
131 % 10 = 1
So 35970-31-1 is a valid CAS Registry Number.

35970-31-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-1-(2,3-dihydro-1,4-benzodioxin-6-yl)ethanone,hydrochloride

1.2 Other means of identification

Product number -
Other names 2-Amino-3',4'-(ethylenedioxy)acetophenone HCl

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:35970-31-1 SDS

35970-31-1Relevant articles and documents

A novel method for preparing Eligulstat through chiral resolution

Chu, Weiming,Du, Jianxun,Feng, Wenhua,Ma, Chunying,Zhang, Mengmeng

, (2020)

Eliglustat is a ceramide glucosyltransferase inhibitor work as first line oral therapy for adults with Gaucher disease type 1 (a rare disease) at present. Although the eliglustat in enantiomerically pure forms is obtained by asymmetric syntheses, the reported methods suffer from many limits when it comes to industrial applications. Therefore, the preparation of a racemic mixture followed by resolution can still be a viable and straightforward alternative, especially when it could be adapted to large scale. Herein, we developed an effective and practical synthetic route to prepare stereoisomers mixture of eliglustat, and a novel chiral resolution method to prepare eliglustat. Using 1,1′-Binaphthyl-2,2′-diyl -hydrogenphosphate (BNDHP) as resolution reagent, optical pure eliglustat (e.e. >99%, 13.97% total yield) could be obtained after recrystallization.

Amino ceramide-like compounds and therapeutic methods of use

-

, (2008/06/13)

Novel amino ceramide-like compounds are provided which inhibit glucosyl ceramide (GlcCer) formation by inhibiting the enzyme GlcCer synthase, thereby lowering the level of glycosphingolipids. The compounds of the present invention have improved GlcCer syn

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