71787-51-4 Usage
Description
1-(2-bromophenyl)but-3-en-1-ol, also known as 2-bromo-1-(3-butene-1-ol), is a chemical compound characterized by a butenol molecule with a bromine-substituted phenyl group attached to one end. It possesses the molecular formula C10H11BrO and exhibits aromatic and organic functional group properties, making it a versatile compound in various applications.
Uses
Used in Organic Chemistry Research:
1-(2-bromophenyl)but-3-en-1-ol is used as a research compound in the field of organic chemistry for studying its aromatic and organic functional group properties. Its unique structure allows for the exploration of various chemical reactions and interactions with other compounds.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 1-(2-bromophenyl)but-3-en-1-ol is used as a starting material for the synthesis of various pharmaceuticals and organic compounds. Its bromine-substituted phenyl group and butenol structure provide a foundation for the development of new drugs and medicinal agents.
Used in Chemical Synthesis:
1-(2-bromophenyl)but-3-en-1-ol is also utilized in the synthesis of other organic compounds, contributing to the development of new materials and products in various industries, such as plastics, dyes, and coatings. Its unique structure and properties make it a valuable building block for creating novel compounds with specific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 71787-51-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,7,8 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 71787-51:
(7*7)+(6*1)+(5*7)+(4*8)+(3*7)+(2*5)+(1*1)=154
154 % 10 = 4
So 71787-51-4 is a valid CAS Registry Number.
71787-51-4Relevant articles and documents
SYNTHESIS OF 4,8-DIHYDROXY-3-METHYL-5,6-BENZO-2-OXABICYCLOOCT-5-ENE
Sudani, Mineichi,Takeuchi, Yoshio,Yoshii, Eiichi,Kometani, Tadashi
, p. 4253 - 4256 (1981)
The title compound having the same relative configuration as granaticin(1) and U-58,431(2) was prepared either by dehydrogenative cyclization of the precursor 9a or by pinacol cyclization of the dicarbonyl compound 15.
Cationic Cobalt Porphyrin-Catalyzed Allylation of Aldehydes with Allyltrimethylsilanes
Tomifuji, Rei,Masuda, Shota,Kurahashi, Takuya,Matsubara, Seijiro
supporting information, p. 3834 - 3837 (2019/05/24)
Cationic cobalt porphyrin-catalyzed allylation of aldehydes with allyltrimethylsilanes is developed. The formation of the aldehyde-cobalt porphyrin complex, the key intermediate for the addition of allylsilanes, is confirmed by theoretical studies and syn
Green Organocatalytic Dihydroxylation of Alkenes
Theodorou, Alexis,Triandafillidi, Ierasia,Kokotos, Christoforos G.
, p. 1502 - 1509 (2017/04/01)
An inexpensive, green, metal-free one-pot procedure for the dihydroxylation of alkenes is described. H2O2 and 2,2,2-trifluoroacetophenone were employed as the oxidant and organocatalyst, respectively, in this highly sustainable protocol in which a variety of homoallylic alcohols, aminoalkenes, and simple alkenes were converted into the corresponding polyalcohols in good to excellent yields. This process takes advantage of an epoxidation reaction followed by an acidic treatment in which water participates in the ring opening of the in situ prepared epoxide to lead to the desired product.
