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Phenol, 3-(3-butenyloxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

176540-50-4

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176540-50-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 176540-50-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,5,4 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 176540-50:
(8*1)+(7*7)+(6*6)+(5*5)+(4*4)+(3*0)+(2*5)+(1*0)=144
144 % 10 = 4
So 176540-50-4 is a valid CAS Registry Number.

176540-50-4Downstream Products

176540-50-4Relevant academic research and scientific papers

Oligomers as intermediates in ring-closing metathesis

Conrad, Jay C.,Eelman, Melanie D.,Duarte Silva, Joao A.,Monfette, Sebastien,Parnas, Henrietta H.,Snelgrove, Jennifer L.,Fogg, Deryn E.

, p. 1024 - 1025 (2007)

Oligomerization is kinetically favored in RCM reactions catalyzed by RuCl2(PCy3)(IMes)(=CHPh), for a range of unhindered α,ω-dienes leading to large or medium-sized rings, even at dilutions designed to minimize intermolecular reactio

Facile construction of the benzofuran and chromene ring systems via Pd II-catalyzed oxidative cyclization

So, Won Youn,Jeong, Im Eom

, p. 3355 - 3358 (2007/10/03)

(Chemical Equation Presented) We herein report the development of one-pot procedures for the conversion of allyl aryl ethers to 2-methylbenzofurans (via sequential Claisen rearrangement and oxidative cyclization) and for the conversion of aryl homoallyl e

Intramolecular Photochemical Reactions of Bichromophoric 3-(Alkenyloxy)phenols and 1-(Alkenyloxy)-3-(alkyloxy)benzene Derivatives. Acid-Catalyzed Transformations of the Primary Cycloadducts

Hoffmann, Norbert,Pete, Jean-Pierre

, p. 6952 - 6960 (2007/10/03)

Irradiation of 3-(alkenyloxy)phenols and 1-(alkenyloxy)-3-(alkyloxy)benzene derivatives, at λ = 254 nm in acidic media, yields benzocyclobutenes, 3-alkylphenols, 3-alkylanisols, and 4-alkyl-1,2dialkyloxybenzenes depending on the substitution pattern of the aromatic ring and the olefinic side chain. The final products are derived from an intramolecular [2 + 2] photocycloaddition and acidic rearrangements from a common intermediate.

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