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116970-50-4

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116970-50-4 Usage

Chemical Properties

White Crystalline Solid

Check Digit Verification of cas no

The CAS Registry Mumber 116970-50-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,9,7 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 116970-50:
(8*1)+(7*1)+(6*6)+(5*9)+(4*7)+(3*0)+(2*5)+(1*0)=134
134 % 10 = 4
So 116970-50-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H13N3O2S.ClH/c12-5-7-14-17(15,16)11-3-1-2-9-8-13-6-4-10(9)11;/h1-4,6,8,14H,5,7,12H2;1H

116970-50-4SDS

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 H-9

1.2 Other means of identification

Product number -
Other names H-9,DiHCl

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:116970-50-4 SDS

116970-50-4Relevant articles and documents

Preparation method of compound fasudil hydrochloride

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Paragraph 0036; 0048-0049, (2021/09/11)

The invention relates to a novel efficient and economical method for synthesizing fasudil hydrochloride. The method comprises the following steps: carrying outsulfonamide and Boc protection on cheap and easily available ethylenediamine serving as a starting raw material in a synthesis route to obtain an intermediate tert-butyl-(N-(2-aminoethyl)-5-isoquinoline sulfonamide) carbamate (5), and carrying out collapse condensation to obtain fasudil hydrochloride. The method comprises four steps of nucleophilic substitution, deprotection, cyclization and salification. The total yield of the fasudil hydrochloride (1) is 67.1%, and the purity of the fasudil hydrochloride (1) is as high as 99.94%. Compared with a traditional process, high-price homopiperazine and derivatives thereof are prevented from being used as synthesis intermediates in the route, so the method has the advantages that raw materials are cheap and easy to obtain, operation is easy, cost is low, and the process is environmentally friendly and suitable for industrial production.

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