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1H-Indene, 3a,7a-dihydro-4,7-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88044-02-4

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88044-02-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88044-02-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,0,4 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 88044-02:
(7*8)+(6*8)+(5*0)+(4*4)+(3*4)+(2*0)+(1*2)=134
134 % 10 = 4
So 88044-02-4 is a valid CAS Registry Number.

88044-02-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,7-diphenyl-3a,7a-dihydro-1H-indene

1.2 Other means of identification

Product number -
Other names 1H-Indene,3a,7a-dihydro-4,7-diphenyl

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:88044-02-4 SDS

88044-02-4Downstream Products

88044-02-4Relevant academic research and scientific papers

Reactions of the cyclopentadienyl ruthenium complexes (C5R 5)Ru(cod)Cl and [(C5R5)Ru(MeCN) 3]+ (R = H, Me) with phenylacetylene and acetic acid: Unexpected difference in reactivity of CpRu and Cp*Ru complexes

Perekalin, Dmitry S.,Trifonova, Evgeniya A.,Novikov, Valentin V.,Nelyubina, Yulia V.,Kudinov, Alexander R.

, p. 21 - 25 (2013)

Reaction of CpRu(cod)Cl with phenylacetylene and AcOH gives an unusual binuclear ruthenium complex CpRu(μ-σ,η3: η3,σ-C6H3Ph3)RuCp (5, 58% yield) with a bridging acyclic flyover ligand C6H3Ph 3. Under similar conditions [CpRu(MeCN)3]+ undergoes an unexpected cleavage of Cp ligand giving 4,7-diphenyl-3a,7a- dihydroindene (6, 65% yield). In sharp contrast, the pentamethylated congeners Cp*Ru(cod)Cl and [Cp*Ru(MeCN)3]+ react with phenylacetylene and AcOH in catalytic fashion giving 1,4-diphenyl-1-acetoxy-1,3- butadiene. The structures of 5 and 6 were established by X-ray diffraction. The mechanism of Cp ligand cleavage was proposed on the basis of DFT calculations.

SYNTHESIS AND PHOTOCHEMICAL REACTION OF DIELS-ALDER ADDUCT OF PHOSPHOLE OXIDE AND CYCLOPENTADIENE

Tomioka, Hideo,Miura, Shinichi,Izawa, Yasuji

, p. 3353 - 3356 (2007/10/02)

Irradiation of 1-phenylphosphole oxide-cyclopentadiene adduct gave a caged product, whereas similar irradiation of 1,2,5-triphenylphosphole oxide-cyclopentadiene adduct afforded a cleavaged product.

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