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6H-benzo[c]thiochromene is a heterocyclic organic compound characterized by a benzene ring fused with a thiochromene ring, which contains sulfur and oxygen atoms. 6H-benzo[c]thiochromene is a member of the benzothiochromene family and is known for its unique chemical structure that combines the properties of both benzene and thiochromene. It is often found in various chemical research and pharmaceutical applications due to its potential biological activities and diverse chemical reactivity. The compound's structure provides a platform for further functionalization and exploration of its properties in different chemical and biological contexts.

230-04-6

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230-04-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 230-04-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,3 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 230-04:
(5*2)+(4*3)+(3*0)+(2*0)+(1*4)=26
26 % 10 = 6
So 230-04-6 is a valid CAS Registry Number.

230-04-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6H-benzo[c]thiochromene

1.2 Other means of identification

Product number -
Other names 9,10-dihydro-9-thiaphenanthrene

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:230-04-6 SDS

230-04-6Relevant academic research and scientific papers

Reactions with 6H-dibenzo[b,d]thiopyran and 6H-dibenzo[b,d]thiopyran-S,S-dioxide

Unterhalt,Bruening

, p. 1 - 10 (2007/10/03)

6H-Dibenzo[b,d]thiopyran (1) is oxidized to its sulfone 2, and both compounds are reacted to the dialkylaminoalkyl derivatives 3 and 4. Chlorinating and cyanation of 1 give the nitrile 6, which is hydrolized to 7 and esterified to 8. Dialkylaminoalkylation of 8 leads to 9, ethylsulfonation of 4 to 5.

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