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2,2-dimethyl-1-(4-methoxyphenyl)-1,3-propanediol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1181812-29-2

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1181812-29-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1181812-29-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,1,8,1 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1181812-29:
(9*1)+(8*1)+(7*8)+(6*1)+(5*8)+(4*1)+(3*2)+(2*2)+(1*9)=142
142 % 10 = 2
So 1181812-29-2 is a valid CAS Registry Number.

1181812-29-2Downstream Products

1181812-29-2Relevant academic research and scientific papers

Phosphine-oxide-catalyzed Enantioselective Cross-aldol Reactions of Aldehydes with Trichlorosilane as Lewis Acid Promoter

Hanamure, Takuya,Kotani, Shunsuke,Mori, Yoshiki,Nakajima, Makoto

, p. 4780 - 4783 (2020/09/09)

A hypervalent silicon complex between trichlorosilane and a chiral phosphine oxide acts as an effective Lewis acid mediator that successfully promotes highly enantioselective cross-aldol reactions between two aldehydes. The high yielding transformation is

Optical enrichment in enzyme-catalyzed resolution of 1-aryl-2,2-dimethyl-1,3-propanediols

Mukherjee, Chandrani,Mohapatra, Prabhu P.,Youssef, Dani,Jha, Amitabh

, p. 1 - 6 (2017/01/10)

Novozym 435 efficiently catalyzed the chemo-, regio-, and enantioselective transesterification of 1-aryl-2,2-dimethyl-1,3-propanediols in different organic solvents with vinyl acetate as the acetyl donor at room temperature. This enzyme-catalyzed chemical

Novel enantioselective direct aldol-type reaction promoted by a chiral phosphine oxide as an organocatalyst

Kotani, Shunsuke,Shimoda, Yasushi,Sugiura, Masaharu,Nakajima, Makoto

supporting information; experimental part, p. 4602 - 4605 (2009/10/26)

Chiral phosphine oxide successfully catalyzed the direct aldol-type reactions of cyclohexanone derivatives and benzaldehyde derivatives in high stereoselectivities. The reaction mechanism involves the in situ formation of trichlorosilyl enol ethers. The present reaction could be extended to the cross-aldol reactions between two aldehydes.

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