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4-Methylthio-piperidine is a chemical compound that is widely utilized in the pharmaceutical and chemical industries. It is recognized for its sulphur-containing alkyl group, which enhances chemical stability and absorption. 4-METHYTHIO-PIPERIDINE is primarily employed as a chemical intermediate in the synthesis of various medicinal products. Its production method is meticulously designed to optimize purity levels, which is crucial for its effectiveness and safety. Although not highly hazardous, it requires appropriate handling to prevent potential skin or eye irritation.

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  • 767270-41-7 Structure
  • Basic information

    1. Product Name: 4-METHYTHIO-PIPERIDINE
    2. Synonyms: 4-METHYTHIO-PIPERIDINE;4-Meththiopiperidine;4-Methylthiopiperidine;4-(METHYLSULFANYL)PIPERIDINE
    3. CAS NO:767270-41-7
    4. Molecular Formula: C6H13NS
    5. Molecular Weight: 131.23912
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 767270-41-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 202.601 °C at 760 mmHg
    3. Flash Point: 76.331 °C
    4. Appearance: /
    5. Density: 0.998 g/cm3
    6. Vapor Pressure: 0.29mmHg at 25°C
    7. Refractive Index: 1.511
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 9.83±0.10(Predicted)
    11. CAS DataBase Reference: 4-METHYTHIO-PIPERIDINE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 4-METHYTHIO-PIPERIDINE(767270-41-7)
    13. EPA Substance Registry System: 4-METHYTHIO-PIPERIDINE(767270-41-7)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 767270-41-7(Hazardous Substances Data)

767270-41-7 Usage

Uses

Used in Pharmaceutical Industry:
4-Methylthio-piperidine is used as a chemical intermediate for the synthesis of medicines, leveraging its unique sulphur-containing alkyl group to improve the stability and absorption of the resulting pharmaceuticals.
Used in Chemical Industry:
In the chemical sector, 4-Methylthio-piperidine serves as a building block in the production of complex molecules, contributing to the creation of a diverse range of chemical compounds for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 767270-41-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,7,2,7 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 767270-41:
(8*7)+(7*6)+(6*7)+(5*2)+(4*7)+(3*0)+(2*4)+(1*1)=187
187 % 10 = 7
So 767270-41-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H13NS/c1-8-6-2-4-7-5-3-6/h6-7H,2-5H2,1H3

767270-41-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-METHYTHIO-PIPERIDINE

1.2 Other means of identification

Product number -
Other names 4-Meththiopiperidine

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:767270-41-7 SDS

767270-41-7Relevant articles and documents

Studies on new platelet aggregation inhibitors 1. Synthesis of 7-nitro-3,4-dihydroquinoline-2(1H)-one derivatives

Iyobe,Uchida,Kamata,Hotel,Kusama,Harada

, p. 822 - 829 (2001)

A series of 6-cyclic aliphatic amino-7-nitro-3,4-dihydroquinoline-2(1H)-ones were prepared and tested for platelet aggregation inhibitory effect, cardiotonic activity and chronotropic activity. These compounds appeared to show selective inhibitory activity against platelet aggregation. Among them, 6-(4-ethoxycarbonylpiperidino)-7-nitro-3,4-dihydroquinoline-2(1H)-one (22f) showed the most potent inhibitory activity and high selectivity. A divergent synthetic route to 6-cyclic aliphatic amino-7-nitro-3,4-dihydroquinoline-2(1H)-one derivatives has also been investigated.

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