Welcome to LookChem.com Sign In|Join Free

CAS

  • or

6196-94-7

Post Buying Request

6196-94-7 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

6196-94-7 Usage

Description

1-(4-Ethylphenyl)-1-phenylethane, also known as ethylbenzylbenzene, is a colorless liquid chemical compound with the molecular formula C20H20. It is insoluble in water and has a slightly sweet, floral odor.

Uses

Used in Fragrance and Flavor Industry:
1-(4-Ethylphenyl)-1-phenylethane is used as a fragrance and flavoring agent for its slightly sweet, floral odor in various consumer products such as perfumes, colognes, and food additives.
Used in Chemical Synthesis:
1-(4-Ethylphenyl)-1-phenylethane is used as a solvent and a starting material for the synthesis of other organic compounds.
Used in Pharmaceutical Research:
1-(4-Ethylphenyl)-1-phenylethane has been studied for its potential use as an anti-inflammatory and antitumor agent, although further research is needed to confirm its efficacy and safety.
Safety Precautions:
It is important to handle 1-(4-Ethylphenyl)-1-phenylethane with care, as it can be harmful if inhaled, ingested, or comes into contact with the skin.

Check Digit Verification of cas no

The CAS Registry Mumber 6196-94-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,9 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6196-94:
(6*6)+(5*1)+(4*9)+(3*6)+(2*9)+(1*4)=117
117 % 10 = 7
So 6196-94-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H18/c1-3-14-9-11-16(12-10-14)13(2)15-7-5-4-6-8-15/h4-13H,3H2,1-2H3

6196-94-7Relevant articles and documents

Continuous synthesis of organozinc halides coupled to Negishi reactions

Alonso, Nerea,Miller, L. Zane,De M. Muoz, Juan,Alczar, Jesus,McQuade, D. Tyler

supporting information, p. 3737 - 3741 (2015/01/16)

The Negishi cross-coupling is a powerful C-C bond forming reaction. The method is less commonly used relative to other cross-coupling methods in part due to lack of availability of organozinc species. While organozinc species can be prepared, problems wit

Selective one-pot synthesis of various phenols from diarylethanes

Nakamura, Ryota,Obora, Yasushi,Ishii, Yasutaka

supporting information; experimental part, p. 3417 - 3419 (2009/02/05)

Various substituted phenols were selectively synthesized by a one-pot reaction through the NHPI-catalyzed aerobic oxidation of 1,1-diarylethanes followed by treatment with dilute sulfuric acid. The Royal Society of Chemistry.

Selective arylation of exocyclic N-position of 2-pyrimidylnitrenium ion photolytically generated from tetrazolo[1,5-a]pyrimidine in the presence of trifluoroacetic acid

Takeuchi, Hiroshi,Watanabe, Keiichi

, p. 478 - 484 (2007/10/03)

Photo-reactions of tetrazolo[1,5-a]pyrimidine (1) with benzene (2a) and substituted benzenes (2b-f) in the presence of trifluoroacetic acid (TFA) gave 2-(2-, 3- and 4-substituted anilino)pyrimidines (3-5) together with 2-aminopyridine (6) and biphenyl (7) or diarylmethanes (8b, 8c and 8e). From the effect of heavy-atom solvent on the reactions, it is reasonable to assume that 3-5 are formed via a singlet species, but 6-8 via a triplet species. The intermediacy of 2-pyrimidylnitrenium ion is consistent with the evidence derived by the above effect, by a Hammett plot with p = -2.9 and by effects of solvent nucleophilicity and counter-anions. The selective exocyclic N-arylation giving 3-5 is discussed.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 6196-94-7