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Benzenepentanoic acid, b-hydroxy-a-methylene- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

308358-34-1

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308358-34-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 308358-34-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,8,3,5 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 308358-34:
(8*3)+(7*0)+(6*8)+(5*3)+(4*5)+(3*8)+(2*3)+(1*4)=141
141 % 10 = 1
So 308358-34-1 is a valid CAS Registry Number.

308358-34-1Downstream Products

308358-34-1Relevant academic research and scientific papers

Diastereoselective peroxidation of derivatives of Baylis–Hillman adducts

Zuckerman, Dylan S.,Woerpel

supporting information, p. 4118 - 4129 (2019/06/24)

Cyclic derivatives of Baylis–Hillman adducts were synthesized. Cobalt-catalyzed peroxidation of these cyclic lactones afforded silyl peroxides in diastereomeric ratios ranging from 91:9 to 97:3.

2 H-Chromene-3-carboxylic Acid Synthesis via Solvent-Controlled and Rhodium(III)-Catalyzed Redox-Neutral C-H Activation/[3 + 3] Annulation Cascade

Zhou, Zhi,Bian, Mengyao,Zhao, Lixin,Gao, Hui,Huang, Junjun,Liu, Xiawen,Yu, Xiyong,Li, Xingwei,Yi, Wei

supporting information, p. 3892 - 3896 (2018/07/22)

An efficient and redox-neutral synthesis of 2H-chromene-3-carboxylic acids from N-phenoxyacetamides and methyleneoxetanones has been realized via a solvent-controlled and rhodium(III)-catalyzed C-H activation/unusual [3 + 3] annulation sequence. This tran

Pd-Catalyzed Acyl C-O Bond Activation for Selective Ring-Opening of α-Methylene-β-lactones with Amines

Malapit, Christian A.,Caldwell, Donald R.,Sassu, Nicole,Milbin, Samuel,Howell, Amy R.

supporting information, p. 1966 - 1969 (2017/04/28)

A Pd-catalyzed ring-opening of β-lactones with various types of amines (primary, secondary, and aryl) to provide β-hydroxy amides with excellent selectivity toward acyl C-O bond cleavage is reported. The utility of this protocol is demonstrated in an asym

Unusual, strained heterocycles: 3-Alkylidene-2-methyleneoxetanes from Morita-Baylis-Hillman-type adducts

Martinez, Isamir,Andrews, Alexander E.,Emch, Joseph D.,Ndakala, Albert J.,Wang, Jun,Howell, Amy R.

, p. 399 - 402 (2007/10/03)

(Matrix presented) 3-Alkylidene-2-methyleneoxetanes have been prepared by treating α-alkylidene-β-lactones, derived from Morita-Baylis-Hillman-type adducts, with dimethyltitanocene. Preliminary studies of the reactivity of these little known, strained het

A novel precipitating auxiliary approach to the purification of Baylis-Hillman adducts

Bosanac,Wilcox

, p. 1618 - 1619 (2007/10/03)

Diaryl alkene alcohol 1 is a 'precipiton', a precipitating auxiliary that is used to aid the isolation of Baylis-Hillman adducts.

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