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(3S*,4S*)-4-methyl-3-phenylhex-5-en-3-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

128081-15-2

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128081-15-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128081-15-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,0,8 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 128081-15:
(8*1)+(7*2)+(6*8)+(5*0)+(4*8)+(3*1)+(2*1)+(1*5)=112
112 % 10 = 2
So 128081-15-2 is a valid CAS Registry Number.

128081-15-2Downstream Products

128081-15-2Relevant academic research and scientific papers

First preparation of allyl vanadium reagents in a mixed solvent of THF and HMPA (HMPA = hexamethylphosphoric triamide) and their application to allylation of carbonyl compounds

Kataoka, Yasutaka,Makihira, Isamu,Tani, Kazuhide

, p. 7083 - 7086 (1996)

Allylation of carbonyl compounds with allyl bromide mediated by a vanadium(II) complex in a mixed solvent of THF and HMPA (HMPA = hexamethylphosphoric triamide) has been accomplished. Coordination of HMPA to a vanadium metal is essential for the stabilization of the allyl vanadium species.

Direct use of 1,3-dienes for the allylation of ketones: Via catalytic hydroindation

Miyamoto, Shinji,Shibata, Ikuya,Suzuki, Itaru,Yagi, Kensuke

, p. 6030 - 6034 (2020/02/26)

In this study, in situ catalytically generated allylic indium from 1,3 dienes and InCl2H was developed for use in the allylation of ketones. This protocol resulted in the unprecedented establishment of a successive combining of quaternary C-C b

Highly diastereoselective addition of allyltitanocenes to ketones

Yatsumonji, Yasutaka,Nishimura, Takuya,Tsubouchi, Akira,Noguchi, Keiichi,Takeda, Takeshi

experimental part, p. 2680 - 2686 (2009/11/30)

The reaction of allyltitanocenes, generated by the reductive titanation of allylic sulfides or allylic alcohol derivatives with a titanocene(II) species, with phenyl and sterically hindered alkyl methyl ketones produced and tertiary homoallylic alcohols w

A Case of Highly Diastereoselective Addition to Unsymmetrical Ketones: lk-Addition of (2-Alkenyl)triphenoxytitanium Derivatives

Seebach, Dieter,Widler, Leo

, p. 1972 - 1981 (2007/10/02)

(2-Butenyl)-, (4-methyl-2-pentenyl)-, and (2-heptenyl)triphenoxytitanium (2a-c) add to dialkyl, alkyl aryl-, and alkinyl aryl ketones to give high yields of tertiary homoallylic alcohols (5-12), which are diastereomerically enriched up to 98percent.Config

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