Welcome to LookChem.com Sign In|Join Free
  • or
(E)-1-Phenyl-2-vinyl-pent-3-en-1-ol is a complex organic compound with the molecular formula C13H14O. It is a conjugated diene, featuring a phenyl group attached to a vinyl group, which in turn is connected to a pent-3-en-1-ol chain. This molecule is characterized by its unique structure, which includes a double bond between the phenyl and vinyl groups, and another double bond in the pent-3-en-1-ol chain. The "E" in its name indicates that the double bonds are in a trans configuration, meaning the substituents on the double bonds are on opposite sides of the molecule. (E)-1-Phenyl-2-vinyl-pent-3-en-1-ol is of interest in organic chemistry due to its potential applications in the synthesis of various pharmaceuticals and other chemical products.

78377-36-3

Post Buying Request

78377-36-3 Suppliers

Recommended suppliers

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

78377-36-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78377-36-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,3,7 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 78377-36:
(7*7)+(6*8)+(5*3)+(4*7)+(3*7)+(2*3)+(1*6)=173
173 % 10 = 3
So 78377-36-3 is a valid CAS Registry Number.

78377-36-3Downstream Products

78377-36-3Relevant academic research and scientific papers

Enantioselective syntheses of 1,4-pentadien-3-yl carbinols via br?nsted acid catalysis

Gao, Shang,Chen, Ming

, p. 400 - 404 (2020)

An asymmetric addition of substituted 1,3-pentadienylboronates to aldehydes via Br?nsted acid catalysis is reported. Under the developed conditions, a variety of synthetically useful 1,4-pentadien-3-yl carbinols were obtained in good yields with high enan

Cobalt-Catalyzed Diastereo- And Enantioselective Reductive Allyl Additions to Aldehydes with Allylic Alcohol Derivatives via Allyl Radical Intermediates

Wang, Lei,Wang, Lifan,Li, Mingxia,Chong, Qinglei,Meng, Fanke

, p. 12755 - 12765 (2021/08/30)

Catalytic generation of ambiphilic π-allyl-metal complexes and their utility in enantioselective transformations constitutes a powerful approach for introduction of allyl groups to a molecule. Herein an unprecedented cobalt-catalyzed highly site-, diastereo-, and enantioselective protocol for stereoselective formation of nucleophilic allyl-Co(II) complexes followed by addition to aldehydes is presented. The reaction features diastereo- and enantioconvergent conversion of easily accessible allylic alcohol derivatives to diversified enantioenriched homoallylic alcohols with a remarkably broad scope of allyl groups that can be introduced. Mechanistic studies indicated that allyl radical intermediates were involved in this process. These new discoveries establish a new strategy for development of enantioselective transformations through capture of radicals by chiral Co complexes, pushing forward the frontier of Co complexes for enantioselective catalysis.

STEREOSELECTIVE ACYCLIC SYNTHESIS VIA ALLYLMETALS: STRUCTURAL DEPENDENCE IN A LEWIS-ACID CATALYZED ADDITION OF ALLYLTINS TO ALDEHYDES

Koreeda, Masato,Tanaka, Yoshio

, p. 1299 - 1302 (2007/10/02)

Lewis-acid catalyzed reaction of allyltins with aldehydes at -78 deg C provide homoallyl alcohols with high stereoselectivity; 2-alkenyltins in general provide erythro adducts preferentially with an erithro/threo ratio greater than 12/1, whereas only thre

CHROMIUM(II) MEDIATED THREO SELECTIVE SYNTHESIS OF HOMOALLYL ALCOHOLS

Hiyama, Tamejiro,Kimura, Keizo,Nozaki, Hitosi

, p. 1037 - 1040 (2007/10/02)

Remarkable threo selectivity is observed in the reaction of aldehydes with trans- and cis-1-bromo-2-butene with the aid of chromium(II) salts.Solvent effect as well as the synthetic application 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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 78377-36-3