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Butane, 2,2-diphenyl-, also known as 2,2-diphenylbutane, is an organic compound with the chemical formula C18H20. It is a colorless, crystalline solid that is insoluble in water but soluble in organic solvents. Butane, 2, 2-diphenyl- is characterized by a butane chain with two phenyl groups attached to the second carbon atom. It is used in the synthesis of various organic compounds and as a chemical intermediate in the pharmaceutical and chemical industries. Due to its relatively low reactivity, 2,2-diphenylbutane is considered a stable compound, but it should still be handled with care due to its potential health and environmental impacts.

5223-61-0

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5223-61-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5223-61-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,2 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5223-61:
(6*5)+(5*2)+(4*2)+(3*3)+(2*6)+(1*1)=70
70 % 10 = 0
So 5223-61-0 is a valid CAS Registry Number.

5223-61-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenylbutan-2-ylbenzene

1.2 Other means of identification

Product number -
Other names Butane,2-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:5223-61-0 SDS

5223-61-0Relevant academic research and scientific papers

Zr-catalyzed coupling reaction of alkyl halides, tosylates, and sulfates with β-phenethyl Grignard reagents via styrene-zirconate intermediates

Terao, Jun,Begum, Shameem Ara,Oda, Akihiro,Kambe, Nobuaki

, p. 1783 - 1786 (2007/10/03)

β-Phenethylmagnesium chlorides react with alkyl halides, tosylates, and sulfates in the presence of a catalytic amount of Cp2ZrCl 2 to afford 2-arylalkanes via alkylation of styrene-zirconate intermediates at the benzylic position. Competitive reaction using mixtures of alkyl halides (alkyl-X; X = F, Cl, Br) showed that the reactivities of the halides increase in the order of alkyl-Cl alkyl-F alkyl-Br with the relative rates of 1:19:428. Georg Thieme Verlag Stuttgart.

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