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38109-75-0

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38109-75-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38109-75-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,1,0 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 38109-75:
(7*3)+(6*8)+(5*1)+(4*0)+(3*9)+(2*7)+(1*5)=120
120 % 10 = 0
So 38109-75-0 is a valid CAS Registry Number.

38109-75-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name E-4-phenyl-4-trimethylsiloxy-3-buten-2-one

1.2 Other means of identification

Product number -
Other names 4-Phenyl-4-(trimethylsilyloxy)-3-buten-2-on

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:38109-75-0 SDS

38109-75-0Relevant articles and documents

REACTIONS OF CYANOTRIMETHYLSILANE WITH β-DIKETONES

Gostevskii, B. A.,Vyazankina, O. A.,Vyazankin, N. S.

, p. 1659 - 1662 (2007/10/02)

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Silylation of 1,3-Dicarbonyl Compounds with 2-Oxo-3-trimethylsilyltetrahydro-1,3-oxazole

Aizpurua, Jesus Mari,Palomo, Claudio

, p. 280 - 281 (2007/10/02)

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A Novel Cycloaromatization Reaction. Regiocontrolled Synthesis of Substituted Methyl Salicylates

Chan, Tak-Hang,Brownbridge, Peter

, p. 3534 - 3538 (2007/10/02)

A new method of constructing six-membered rings, involving the condensation of two three-carbon units, one with two nucleophilic sites and the other containing two electrophilic sites, is reported.The regiochemistry of the reaction is controlled by the differential reactivities of these sites. 1,3-Bis(trimethylsiloxy)-1-methoxybuta-1,3-diene (1) constitutes the three-carbon fragment with two nucleophilic sites.Condensation of 1 with various equivalents of β-dicarbonyl compounds and titanium tetrachloride gave substituted methyl salicylates.The regiochemistry is controlled by the order of reactivity of the electrophilic sites, which is conjugate position of enone > ketone > monothioacetal, acetal.

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