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4,7-Methano-1H-inden-1-one, 3a,4,7,7a-tetrahydro-3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

132272-90-3

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132272-90-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132272-90-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,2,7 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 132272-90:
(8*1)+(7*3)+(6*2)+(5*2)+(4*7)+(3*2)+(2*9)+(1*0)=103
103 % 10 = 3
So 132272-90-3 is a valid CAS Registry Number.

132272-90-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,7-Methano-1H-inden-1-one, 3a,4,7,7a-tetrahydro-3-phenyl-

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:132272-90-3 SDS

132272-90-3Relevant academic research and scientific papers

Synthesis and application of β-substituted Pauson-Khand adducts: Trifluoromethyl as a removable steering group

Aiguabella, Nuria,Del Pozo, Carlos,Verdaguer, Xavier,Fustero, Santos,Riera, Antoni

, p. 5355 - 5359 (2013/06/05)

Against the rules: The synthesis of the previously unknown β-substituted regioisomers of the intermolecular Pauson-Khand reaction of terminal alkynes is reported. This regiochemistry was achieved by using the trifluoromethyl group as a removable directing group on the alkyne. Copyright

Bis(cyclopentadienyl)tetracarbonyldimolybdenum-alkyne Complexes Mediated Cycloaddition: the Formation of 3-Substituted Cyclopentenone Derivatives

Mukai, Chisato,Uchiyama, Masahiko,Hanaoka, Miyoji

, p. 1014 - 1015 (2007/10/02)

On heating, bis(cyclopentadienyl)tetracarbonyldimolybdenum-alkyne complexes undergo a cycloaddition with norbornadiene or norbornene to afford the corresponding 3-substituted cyclopentenone derivatives, which could hardly be obtained in the cobalt-complexed alkyne-mediated Pauson-Khand reaction.

Novel Acid-catalysed Rearrangement of 4-Substituted Pentacyclo2,5.03,9.04,8>decan-6-ones; X-Ray Molecular Structure of 1-Phenylpentacyclo2,10.03,8.05,7>decan-4-one

Ogino, Toshio,Awano, Kazuyuki,Fukazawa, Yoshimasa

, p. 1735 - 1738 (2007/10/02)

4-Substituted pentacyclo2,5.03,9.04,8>decan-6-one derivatives 2a and b undergo a novel acid- or Ag+-catalysed rearrangement to the hitherto unknown pentacyclo2,10.03,8.05,7>

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