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107866-55-7

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107866-55-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107866-55-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,8,6 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 107866-55:
(8*1)+(7*0)+(6*7)+(5*8)+(4*6)+(3*6)+(2*5)+(1*5)=147
147 % 10 = 7
So 107866-55-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H14O3/c1-9(13)14-11-6-4-10(5-7-11)3-2-8-12/h4-7,12H,2-3,8H2,1H3

107866-55-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(3-hydroxypropyl)phenyl] acetate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:107866-55-7 SDS

107866-55-7Relevant articles and documents

Heterogeneous catalysis in acetylation of alcohols and phenols promoted by zirconium sulfophenyl phosphonate

Curini, Massimo,Epifano, Francesco,Marcotullio, Maria Carla,Rosati, Ornelio,Rossi, Monia

, p. 1319 - 1329 (2000)

Layered zirconium sulfophenyl phosphonate was found to be an efficient heterogeneous catalyst for the acetylation of alcohols and phenols.

Synthesis of tetrahydropyranyl diarylheptanoids from Dioscorea villosa

Kantee, Kawalee,Rukachaisirikul, Vatcharin,Tadpetch, Kwanruthai

supporting information, p. 3505 - 3509 (2016/07/15)

Concise syntheses of four tetrahydropyranyl diarylheptanoids isolated from Dioscorea villosa have been described. The key features include Prins cyclization to construct the tetrahydropyran cores, Keck asymmetric allylation, and Mitsunobu inversion. Optimization of the Prins cyclization conditions in order to minimize racemization has been described. Our syntheses also confirmed the absolute stereochemistry of the natural products.

Synthesis of a novel diarylheptanoid isolated from Zingiber officinale

Parker, Gregory D.,Seden, Peter T.,Willis, Christine L.

scheme or table, p. 3686 - 3689 (2009/10/04)

Syntheses of 4-acetoxy-2,6-disubstituted tetrahydropyrans via Prins cyclisation of homoallylic alcohols with benzylic aldehydes are described and the methodology is applied in the total synthesis of diarylheptanoid 1 confirming both the structure and abso

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