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CAS

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23706-25-4

1H-Indole-3-ylthio cyanide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 23706-25-4 Structure

  • Basic information

    1. Product Name: 1H-Indole-3-ylthio cyanide
    2. Synonyms: 1H-Indol-3-yl thiocyanate;1H-Indole-3-ylthio cyanide;3-(Cyanothio)-1H-indole;3-Thiocyanato-1H-indole;3-Thiocyanatoindole;Thiocyanic acid 1H-indol-3-yl ester
    3. CAS NO:23706-25-4
    4. Molecular Formula: C9H6N2S
    5. Molecular Weight: 174.2223
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 23706-25-4.mol

  • Chemical Properties

    1. Melting Point: 73-76 °C
    2. Boiling Point: 389.4°Cat760mmHg
    3. Flash Point: 189.3°C
    4. Appearance: /
    5. Density: 1.36g/cm3
    6. Vapor Pressure: 2.86E-06mmHg at 25°C
    7. Refractive Index: 1.724
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 14.82±0.30(Predicted)
    11. CAS DataBase Reference: 1H-Indole-3-ylthio cyanide(CAS DataBase Reference)
    12. NIST Chemistry Reference: 1H-Indole-3-ylthio cyanide(23706-25-4)
    13. EPA Substance Registry System: 1H-Indole-3-ylthio cyanide(23706-25-4)

  • 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: 23706-25-4(Hazardous Substances Data)

23706-25-4 Usage

Structure

Bicyclic, with a cyanide derivative of indole

Type

Chemical compound

Usage

Various chemical reactions and processes

Potential applications

Pharmaceutical research and organic synthesis

Unique properties

Valuable reagent in the development of new drugs and industrial products

Interest

Medicinal chemistry for the development of new pharmaceutical compounds

Check Digit Verification of cas no

The CAS Registry Mumber 23706-25-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,7,0 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 23706-25:
(7*2)+(6*3)+(5*7)+(4*0)+(3*6)+(2*2)+(1*5)=94
94 % 10 = 4
So 23706-25-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H6N2S/c10-6-12-9-5-11-8-4-2-1-3-7(8)9/h1-5,11H

23706-25-4SDS

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 1H-indol-3-yl thiocyanate

1.2 Other means of identification

Product number -
Other names 3-thiocyanato 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:23706-25-4 SDS

23706-25-4Relevant articles and documents

Catalytic Thiourea Promoted Electrophilic Thiocyanation of Indoles and Aromatic Amines with NCS/NH4SCN

Wang, Cancan,Wang, Zhonghao,Wang, Liang,Chen, Qun,He, Mingyang

supporting information, p. 1081 - 1085 (2016/11/25)

A simple and efficient protocol for the electrophilic thiocyanation of indoles and aromatic amines with thiourea/NCS/NH4SCN system has been developed. The major features of the present procedure are the mild conditions, good yields, short reaction times, and the use of inexpensive and readily available organocatalyst. Moreover, N-chlorosuccinimide (NCS) was found to be indispensable, and thiourea could greatly promote the reaction.

Ferric(III) chloride-promoted electrophilic thiocyanation of aromatic and heteroaromatic compounds

Yadav,Reddy,Krishna,Suresh Reddy,Narsaiah

, p. 961 - 964 (2007/10/03)

Indoles, oxindoles and aromatic amino compounds undergo smooth thiocyanation with ammonium thiocyanate in the presence of anhydrous FeCl 3 in dichloromethane under mild conditions to afford the corresponding 3-indolyl and 4-aryl thiocyanates, respectively, in high yields with excellent selectivity. The use of ferric chloride makes it quite simple, more convenient and practical. This new method offers several advantages such as high conversions, cleaner reaction profiles, short reaction times, and the use of inexpensive and readily available catalyst. Georg Thieme Verlag Stuttgart.

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