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3-(9'-Fluorenyl)-1,3,4,5,6,7-hexahydrobenzothiophen is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76390-46-0

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76390-46-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76390-46-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,3,9 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 76390-46:
(7*7)+(6*6)+(5*3)+(4*9)+(3*0)+(2*4)+(1*6)=150
150 % 10 = 0
So 76390-46-0 is a valid CAS Registry Number.

76390-46-0SDS

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 3-(9'-Fluorenyl)-1,3,4,5,6,7-hexahydrobenzo[c]thiophen

1.2 Other means of identification

Product number -
Other names -

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:76390-46-0 SDS

76390-46-0Upstream product

76390-46-0Relevant academic research and scientific papers

Organosulfur Compounds, L. - 2H-Thiopyrans and Dihydro-2H-thiopyrans, Synthons for Thiophenes

Praefcke, Klaus,Weichsel, Christian

, p. 1604 - 1619 (2007/10/02)

2H-Thiopyran derivatives yield thiophenes on pyrolysis at 240-260 deg C.The influence of substitution in positions 3 to 6 of the 2H-thiopyrans on these new thermal rearrangement and fragmentation reactions is dealt with, and some proposed mechanisms are discussed in detail.A novel three-step synthesis of thiophenes from carbonyl compounds via the corresponding thiones, their -cycloaddition with 1,3-dienes with formation of dihydro-2H-thiopyrans and subsequent thermal conversion is described.In this reaction sequence, whose scope and limitations are outlined, t he thiocarbonyl compound contributes the sulfur and the 1,3-diene the carbon skeleton of the desired thiophenes.

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