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2-[[1-(METHYLAMINO)-2-NITROETHENYL]AMINO]-ETHANETHIOL, also known as Methylaminoethanethiol nitrosyl, is a chemical compound with the formula C5H11N3O2S. It is a yellow crystalline powder that is used in the synthesis of drugs, dyes, and other organic compounds. 2-[[1-(METHYLAMINO)-2-NITROETHENYL]AMINO]-ETHANETHIOL is known for its ability to inhibit the growth of cancer cells and has potential applications in anti-cancer therapies. It is also used as a building block in the synthesis of various pharmaceuticals with anti-tumor and anti-inflammatory properties. Additionally, it has been investigated for its potential in treating certain bacterial infections. However, due to its toxic and reactive nature, it requires proper handling and storage to avoid any adverse effects on human health and the environment.

66357-41-3

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66357-41-3 Usage

Uses

Used in Pharmaceutical Industry:
2-[[1-(METHYLAMINO)-2-NITROETHENYL]AMINO]-ETHANETHIOL is used as a building block for the synthesis of pharmaceuticals with anti-tumor and anti-inflammatory properties. Its ability to inhibit the growth of cancer cells makes it a promising candidate for anti-cancer therapies.
Used in Drug Synthesis:
2-[[1-(METHYLAMINO)-2-NITROETHENYL]AMINO]-ETHANETHIOL is used as a key intermediate in the synthesis of various drugs, including those with potential applications in treating bacterial infections.
Used in Dye Industry:
2-[[1-(METHYLAMINO)-2-NITROETHENYL]AMINO]-ETHANETHIOL is used in the synthesis of dyes, contributing to the development of new colorants for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 66357-41-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,3,5 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 66357-41:
(7*6)+(6*6)+(5*3)+(4*5)+(3*7)+(2*4)+(1*1)=143
143 % 10 = 3
So 66357-41-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H11N3O2S/c1-6-5(4-8(9)10)7-2-3-11/h4,6-7,11H,2-3H2,1H3/b5-4+

66357-41-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[[1-(methylamino)-2-nitroethenyl]amino]ethanethiol

1.2 Other means of identification

Product number -
Other names N-thioethyl-N'-methyl-2-nitro-1,1-ethendiamine

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:66357-41-3 SDS

66357-41-3Downstream Products

66357-41-3Relevant academic research and scientific papers

Method for synthesizing ranitidine

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Paragraph 0040; 0041; 0051; 0052; 0062; 0063; 0073; 0074, (2017/10/09)

A method for synthesizing ranitidine includes following steps: 1), dropwise adding sodium hydroxide water solution into 1, 1, 2-trichloroethane at 30-35 DEG C for reaction to obtain vinylidene chloride, wherein a mass ratio of 1, 1, 2-trichloroethan to sodium hydroxide is 1:0.3-0.33; 2), dropwise adding vinylidene chloride into mixed acid of concentrated hydrochloric acid and concentrated nitric acid at 20-25 DEG C for reaction for 2-4h, wherein a consumption ratio of vinylidene chloride to the mixed acid is 1:2-3; 3), adding cysteamine hydrochloride into sodium hydroxide and potassium hydroxide solution, and dropwise adding a product of the step 2) at 50-55 DEG C to obtain a closed-loop product; 4), enabling the closed-loop product to react with alcohol or methanol solution at room temperature for 14-18h to obtain an open-loop product; 5), adding the open-loop product and 2-[(dimethylamino)methyl]-5 chloromethyl-furan into potassium hydroxide or sodium hydroxide water solution for reaction at 40-50 DEG C for 2-4h to obtain ranitidine. The method lowers potential safety hazards and is simple and easy for industrial production.

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