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6-ISOCYANATO-1-METHYL-1H-INDOLE 97+% is a chemical compound with a purity of 97% or higher. It is an isocyanate derivative of 1-methyl-1H-indole and has a molecular formula of C9H8N2O. This versatile chemical is known for its unique structure and reactivity, making it a valuable component in various scientific and technological applications.

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  • 898289-03-7 Structure
  • Basic information

    1. Product Name: 6-ISOCYANATO-1-METHYL-1H-INDOLE 97+%
    2. Synonyms: 6-ISOCYANATO-1-METHYL-1H-INDOLE 97+%;6-ISOCYANATO-1-METHYL-1H-INDOLE;6-Isocyanato-1-methylindole;6-Isocyanato-1-methylindole 97%;6-Isocyanato-1-methylindole97%;1-Methyl-1H-indol-6-yl isocyanate 97%;1-Methyl-1H-indol-6-ylisocyanate97%
    3. CAS NO:898289-03-7
    4. Molecular Formula: C10H8N2O
    5. Molecular Weight: 172.18332
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 898289-03-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 297.312°C at 760 mmHg
    3. Flash Point: 133.61°C
    4. Appearance: /
    5. Density: 1.16g/cm3
    6. Vapor Pressure: 0.001mmHg at 25°C
    7. Refractive Index: 1.606
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. Sensitive: Moisture Sensitive/Lachrymatory
    11. CAS DataBase Reference: 6-ISOCYANATO-1-METHYL-1H-INDOLE 97+%(CAS DataBase Reference)
    12. NIST Chemistry Reference: 6-ISOCYANATO-1-METHYL-1H-INDOLE 97+%(898289-03-7)
    13. EPA Substance Registry System: 6-ISOCYANATO-1-METHYL-1H-INDOLE 97+%(898289-03-7)
  • Safety Data

    1. Hazard Codes: C,T
    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: 898289-03-7(Hazardous Substances Data)

898289-03-7 Usage

Uses

Used in Pharmaceutical Industry:
6-ISOCYANATO-1-METHYL-1H-INDOLE 97+% is used as a building block for the synthesis of various organic compounds, particularly in the development of new pharmaceuticals. Its unique structure and reactivity contribute to the creation of innovative drug candidates.
Used in Chemical Industry:
In the chemical industry, 6-ISOCYANATO-1-METHYL-1H-INDOLE 97+% is utilized for the production of dyes, pigments, and other industrial chemicals. Its versatility allows it to be a key component in the formulation of a wide range of products.
Used in Medicinal Chemistry and Drug Discovery:
6-ISOCYANATO-1-METHYL-1H-INDOLE 97+% is recognized for its potential applications in medicinal chemistry and drug discovery. Its unique properties make it a promising candidate for the development of new therapeutic agents and the advancement of pharmaceutical research.

Check Digit Verification of cas no

The CAS Registry Mumber 898289-03-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,8,2,8 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 898289-03:
(8*8)+(7*9)+(6*8)+(5*2)+(4*8)+(3*9)+(2*0)+(1*3)=247
247 % 10 = 7
So 898289-03-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H8N2O/c1-12-5-4-8-2-3-9(11-7-13)6-10(8)12/h2-6H,1H3

898289-03-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-isocyanato-1-methylindole

1.2 Other means of identification

Product number -
Other names 6-Isocyanato-1-methyl-1H-indole

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:898289-03-7 SDS

898289-03-7Downstream Products

898289-03-7Relevant articles and documents

Synthesis of highly substituted indole alkaloid species via [4+1] cyclization of nucleophilic carbenes and indole isocyanates

Rigby, James H.,Burke, Patrick J.

, p. 643 - 653 (2007/10/03)

Thermally induced [4+1] cyclization between indole isocyanates and dimethoxycarbene or bis(propylthio)carbene has been achieved with good chemical efficiency. The methodology provides rapid access to fused pyrroloindole substructures commonly found in a variety of indole alkaloid natural products.

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