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  • 63139-97-9 Structure
  • Basic information

    1. Product Name: (2-METHYL-1,3-THIAZOL-5-YL)METHYLAMINE
    2. Synonyms: (2-METHYL-1,3-THIAZOL-5-YL)METHYLAMINE;(2-Methylthiazol-5-yl)MethanaMine;C-(2-Methyl-thiazol-5-yl)-methylamine;(2-Methyl-1,3-thiazol-5-yl)methanamine
    3. CAS NO:63139-97-9
    4. Molecular Formula: C5H8N2S
    5. Molecular Weight: 128.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 63139-97-9.mol
    9. Article Data: 2
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 221.4±15.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.182±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
    8. Solubility: N/A
    9. PKA: 8.26±0.29(Predicted)
    10. CAS DataBase Reference: (2-METHYL-1,3-THIAZOL-5-YL)METHYLAMINE(CAS DataBase Reference)
    11. NIST Chemistry Reference: (2-METHYL-1,3-THIAZOL-5-YL)METHYLAMINE(63139-97-9)
    12. EPA Substance Registry System: (2-METHYL-1,3-THIAZOL-5-YL)METHYLAMINE(63139-97-9)
  • Safety Data

    1. Hazard Codes: Xn
    2. Statements: 22-37/38-41
    3. Safety Statements: 26-39
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 63139-97-9(Hazardous Substances Data)

63139-97-9 Usage

Description

(2-Methyl-1,3-thiazol-5-yl)methylamine is a simple, organic compound composed of various elements such as carbon, hydrogen, nitrogen, and sulfur. It is known for its role in organic synthesis, with a chemical structure that features a thiazole ring, a five-membered aromatic ring containing two non-adjacent heteroatoms (sulfur and nitrogen), to which an amine functional group is attached. Like other amines, this compound has a lone pair of electrons on the nitrogen, allowing it to participate in various chemical reactions.

Uses

Used in Pharmaceutical Industry:
(2-Methyl-1,3-thiazol-5-yl)methylamine is used as a building block or intermediate for drug synthesis, particularly due to its potential for substituent variability and its biological relevance. Its unique structure and reactivity make it a valuable component in the development of new pharmaceutical compounds.
Used in Organic Synthesis:
(2-Methyl-1,3-thiazol-5-yl)methylamine is used as a reagent in various organic synthesis processes, where its thiazole ring and amine functional group can be utilized to form a wide range of chemical products. Its versatility in reactions makes it a useful tool in the synthesis of complex organic molecules.
It is important to handle (2-Methyl-1,3-thiazol-5-yl)methylamine with care, using appropriate safety measures to avoid exposure and potential harm, as with all chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 63139-97-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,1,3 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 63139-97:
(7*6)+(6*3)+(5*1)+(4*3)+(3*9)+(2*9)+(1*7)=129
129 % 10 = 9
So 63139-97-9 is a valid CAS Registry Number.

63139-97-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-methyl-1,3-thiazol-5-yl)methanamine

1.2 Other means of identification

Product number -
Other names 5-(aminomethyl)-2-methylthiazole

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:63139-97-9 SDS

63139-97-9Relevant articles and documents

HEPATITIS B CORE PROTEIN MODULATORS

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Page/Page column 108; 110, (2018/04/13)

The present disclosure provides, in part, compounds having allosteric effector properties against Hepatitis B virus Cp. Also provided herein are methods of treating viral infections, such as hepatitis B, comprising administering to a patient in need thereof a disclosed compound of formula:

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