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17124-82-2

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17124-82-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17124-82-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,2 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17124-82:
(7*1)+(6*7)+(5*1)+(4*2)+(3*4)+(2*8)+(1*2)=92
92 % 10 = 2
So 17124-82-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H13N3S/c1-8(2)3-4-9-5(6)7/h3-4H2,1-2H3,(H3,6,7)

17124-82-2SDS

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 S-(dimethylaminoethyl)isothiourea

1.2 Other means of identification

Product number -
Other names S-(2-dimethylamino-ethyl)-isothiourea

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:17124-82-2 SDS

17124-82-2Downstream Products

17124-82-2Relevant articles and documents

Macrocyclic polyamines as a possible chemical model for histamine H2-receptors

Kimura,Koike,Kodama

, p. 3569 - 5578 (1984)

An 18-membered macrocyclic hexaamine, [18]aneN6, interacts with histamine and its H2-agonist dimaprit at physiological pH to yield stable 1:1 complexes with simultaneous liberation of H+ which mimics the histamine H2-receptor-agonist interaction and the resulting gastric acid secretion. The polyamine H2-receptor model does not interact with the histamine H1-agonist 2-pyridylethylamine. Our model does interact with the H2-antagonists cimetidine, metiamide, famotidine and ranitidine to form more stable 1:1 complexes than with the H2-agonists, which offers a possible chemical model for the pharmacological ability of the H2-antagonists to competitively block H2-receptors and inhibit the gastric acid secretion induced by histamine. The known structural features distinguishing between histamine H1- and H2-agonist, and between histamine H2-agonist and -antagonist are reevaluated in terms of our model.

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