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tetradecyl heptanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29710-33-6

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29710-33-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29710-33-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,7,1 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 29710-33:
(7*2)+(6*9)+(5*7)+(4*1)+(3*0)+(2*3)+(1*3)=116
116 % 10 = 6
So 29710-33-6 is a valid CAS Registry Number.
InChI:InChI=1/C21H42O2/c1-3-5-7-9-10-11-12-13-14-15-16-18-20-23-21(22)19-17-8-6-4-2/h3-20H2,1-2H3

29710-33-6SDS

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 tetradecyl heptanoate

1.2 Other means of identification

Product number -
Other names Heptanoic acid,tetradecyl ester

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:29710-33-6 SDS

29710-33-6Downstream Products

29710-33-6Relevant academic research and scientific papers

Solvent-free esterification of carboxylic acids and alcohols in the presence of silphos [PCl3-n(SiO2)n] as a heterogeneous phosphine reagent

Rao, Ambati Narasimha,Ganesan, Kumaran,Shinde, Chandra Kant

experimental part, p. 2299 - 2308 (2012/06/18)

An efficient solvent-free method for the preparation of esters from various aromatic and aliphatic acids with primary, secondary, and tertiary alcohols using a heterogeneous phosphine reagent, silphos [PCl3-n(SiO 2)n], in good yields is reported.

SYNTHESIS OF 20-IODOEICOSANOIK AND 20--IODOEICOSANOIK ACIDS

Protiva, Jiri,Pecka, Jaroslav,Urban, Jiri,Zima, Jiri

, p. 1546 - 1554 (2007/10/02)

20-Iodoeicosanoic acid (X) was prepared in 9 steps, its carbon cain being constructed from thiophene and ethyl ester chlorides of dodecanedioic and butanedioic acids.Isotope exchange afforded 20--iodoeicosanoic acid required for scintigraphic studies of the myocardium.Desulfuration of the thiophene precursor VIII was accompanied by formation of side products XI-XIX arising by cleavage of the thiophene C-C bonds.Desulfuration of the model compounds XX and XXI has shown that the formation of these products is general.

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