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Ethyl 2-bromononan-1-oate is an organic compound with the chemical formula C11H21BrO2. It is a colorless liquid at room temperature and is soluble in organic solvents. ethyl 2-bromononan-1-oate is a derivative of nonanoic acid, where the carboxylic acid group is esterified with ethanol, and the second carbon atom of the nonane chain is substituted with a bromine atom. Ethyl 2-bromononan-1-oate is primarily used as a synthetic intermediate in the production of various chemicals, pharmaceuticals, and fragrances. It is also employed in the synthesis of specialty polymers and as a reagent in organic chemistry. Due to its reactivity, it is essential to handle ethyl 2-bromononan-1-oate with care, following proper safety protocols.

7425-60-7

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7425-60-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7425-60-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,2 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7425-60:
(6*7)+(5*4)+(4*2)+(3*5)+(2*6)+(1*0)=97
97 % 10 = 7
So 7425-60-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H21BrO2/c1-3-5-6-7-8-9-10(12)11(13)14-4-2/h10H,3-9H2,1-2H3

7425-60-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-bromononanoate

1.2 Other means of identification

Product number -
Other names ethyl 2-bromononanate

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:7425-60-7 SDS

7425-60-7Relevant academic research and scientific papers

Unnatural nucleosides and nucleotides. III. Preparation of 2-14C and 4-14C labelled 5-alkyluracils and 5-alkyl-2'-deoxyuridines

Szabolcs,Kruppa,Sagi,Otvos

, p. 713 - 726 (2007/10/08)

2-14C Labelled 5-alkyluracils were prepared by condensation of the diethylacetals of α-formyl-carbonic acid esters with 14C-thiourea. Compounds labelled at 4-C were synthesized by condensation of the labelled carboxylic acid derivatives with thiourea. β-Anomers of 5-alkyl-2'-deoxyuridines were obtained in a fairly good radiochemical yield. Alkyl substituents ranged from methyl to tetradecyl, isopropyl and tert-butyl.

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