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2-[(2,4,6-Trimethylphenyl)thio]ethanamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 103423-06-9 Structure
  • Basic information

    1. Product Name: 2-[(2,4,6-Trimethylphenyl)thio]ethanamine
    2. Synonyms: 2-[(2,4,6-Trimethylphenyl)thio]ethanamine
    3. CAS NO:103423-06-9
    4. Molecular Formula: C11H17NS
    5. Molecular Weight: 195.32438
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 103423-06-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-[(2,4,6-Trimethylphenyl)thio]ethanamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-[(2,4,6-Trimethylphenyl)thio]ethanamine(103423-06-9)
    11. EPA Substance Registry System: 2-[(2,4,6-Trimethylphenyl)thio]ethanamine(103423-06-9)
  • 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: 103423-06-9(Hazardous Substances Data)

103423-06-9 Usage

Physical state

Colorless to light yellow liquid

Odor

Strong amine odor

Uses

Intermediate in the synthesis of pharmaceuticals and agrochemicals, potential use in the treatment of certain neurological disorders

Health hazards

Irritant effects on the skin, eyes, and respiratory tract, nausea, headache, and dizziness at high concentrations

Safety precautions

Proper handling and use to avoid exposure and potential health hazards

Check Digit Verification of cas no

The CAS Registry Mumber 103423-06-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,4,2 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 103423-06:
(8*1)+(7*0)+(6*3)+(5*4)+(4*2)+(3*3)+(2*0)+(1*6)=69
69 % 10 = 9
So 103423-06-9 is a valid CAS Registry Number.

103423-06-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-<(2,4,6-trimethylphenyl)thio>ethylamine

1.2 Other means of identification

Product number -
Other names 2-(2,4,6-trimethyl-phenylsulfanyl)-ethylamine

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:103423-06-9 SDS

103423-06-9Relevant articles and documents

Inactivation of Cytochrome P-450 during Catalytic Oxidation of a 3-sydnone: N-Vinyl Heme Formation via Insertion into the Fe-N Bond

Montellano de, Paul R. Ortiz,Grab, Lawrence A.

, p. 5584 - 5589 (2007/10/02)

A 3--4-methylsydnone has been synthesized and shown to destroy hepatic microsomal cytochrome P-450 in a time- and NADPH-dependent manner.Enzyme destruction is accompanied by the formation of pyruvic acid and a green hepatic pigment.The pigment has been purified and identified by analytical and spectroscopic methods as a mixture of the four isomers of N-vinylprotoporphyrin IX.The results indicate that enzyme-catalyzed hydroxylation of the sydnone anionic carbon fragments the heterocyclic ring into pyruvic acid and a 2-(arylthio)ethyl diazonium species that reacts with the prosthetic heme group.Internal elimination of the arylthio moiety from a bridged Fe-CHR-N adduct rationalizes the formation of N-vinylprotoporphyrin IX.The results provide strong support for the biological formation of bridged Fe-C-N species and an explanation for some of the biological activities of the sydnones.

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