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3-pentadecanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53346-71-7

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53346-71-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53346-71-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,4 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 53346-71:
(7*5)+(6*3)+(5*3)+(4*4)+(3*6)+(2*7)+(1*1)=117
117 % 10 = 7
So 53346-71-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H32O/c1-3-5-6-7-8-9-10-11-12-13-14-15(16)4-2/h15-16H,3-14H2,1-2H3

53346-71-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name pentadecan-3-ol

1.2 Other means of identification

Product number -
Other names 3-Pentadecanol

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:53346-71-7 SDS

53346-71-7Downstream Products

53346-71-7Relevant academic research and scientific papers

Silver-catalyzed decarboxylative fluorination of aliphatic carboxylic acids in aqueous solution

Yin, Feng,Wang, Zhentao,Li, Zhaodong,Li, Chaozhong

supporting information; experimental part, p. 10401 - 10404 (2012/08/08)

Although fluorinated compounds have found widespread applications in the chemical and materials industries, general and site-specific C(sp3)-F bond formations are still a challenging task. We report here that with the catalysis of AgNO3, various aliphatic carboxylic acids undergo efficient decarboxylative fluorination with SELECTFLUOR reagent in aqueous solution, leading to the synthesis of the corresponding alkyl fluorides in satisfactory yields under mild conditions. This radical fluorination method is not only efficient and general but also chemoselective and functional-group- compatible, thus making it highly practical in the synthesis of fluorinated molecules. A mechanism involvinig Ag(III)-mediated single electron transfer followed by fluorine atom transfer is proposed for this catalytic fluorodecarboxylation.

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