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Cyclopenta[b]thiopyran, octahydro-2,4-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54146-77-9

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54146-77-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54146-77-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,1,4 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54146-77:
(7*5)+(6*4)+(5*1)+(4*4)+(3*6)+(2*7)+(1*7)=119
119 % 10 = 9
So 54146-77-9 is a valid CAS Registry Number.

54146-77-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-diphenyl-2,3,4,4a,5,6,7,7a-octahydrocyclopenta[b]thiopyran

1.2 Other means of identification

Product number -
Other names 3,5-Diphenyl-2-thiabicyclo<4.3.0>nonan

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:54146-77-9 SDS

54146-77-9Downstream Products

54146-77-9Relevant academic research and scientific papers

CATALYTIC AND IONIC REDUCTION OF THE DOUBLE BONDS IN 4H-CYCLOPENTATHIOPYRANS. ISOMERIC 2-THIABICYCLONONANES

Klimenko, S. K.,Tyrina, T. I.,Sorokin, N. N.

, p. 342 - 345 (2007/10/02)

The stereochemical direction in the reduction of the double bonds of monoaryl- and diaryl-substituted 4H-cyclopentathiopyrans during hydrogenation at platinum and during acid-catalyzed disproportionation in trifluoroacetic acid was studied.The structur

REACTIONS OF "SEMICYCLIC" 1,5-DIKETONES WITH HYDROGEN SULFIDE AND TRIFLUOROACETIC ACID

Stolbova, T. V.,Klimenko, S. K.,Kharchenko, V. G.

, p. 170 - 173 (2007/10/02)

The reactions of known and new "semicyclic" 1,5-diketones with hydrogen sulfide and with trifluoroacetic acid were studied.It was shown that under the investigated conditions both 1-aryl- and 1,3-diaryl-substituted diketones form 3R-5R-2-thiabicycloalkane

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