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Benzene, [2-(diethoxymethyl)hexyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16510-48-8

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16510-48-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16510-48-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,5,1 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16510-48:
(7*1)+(6*6)+(5*5)+(4*1)+(3*0)+(2*4)+(1*8)=88
88 % 10 = 8
So 16510-48-8 is a valid CAS Registry Number.

16510-48-8SDS

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 2-Benzylhexanal-diethyl-acetal

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:16510-48-8 SDS

16510-48-8Downstream Products

16510-48-8Relevant academic research and scientific papers

REACTIVITY OF RCu,BF3 AND R2CuLi,BF3 TOWARDS ALLYLIC ACETALS AND ETHERS

Ghribi, A.,Alexakis, A.,Normant, J. F.

, p. 3079 - 3082 (2007/10/02)

Organocopper and cuprate reagents associated with Lewis acids, are highly reactive towards allylic acetals and ethers.Displacements of the alkoxy group occurs by SN2' attack according to the various parameters of the reaction.

REACTIVITY OF α,β-UNSATURATED ACETALS AND KETALS TOWARD ORGANOLITHIUM REAGENTS IN PENTANE

Mioskowski, Charles,Manna, S.,Falck, J. R.

, p. 519 - 522 (2007/10/02)

Depending upon structure and reaction conditions, α,β-unsaturated acetals and ketals react with organolithium reagents in pentane by addition, substitution, or proton abstraction.

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