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4-(benzyloxy)phenyl butanoate is an organic compound with the chemical formula C17H18O3. It is a derivative of phenyl butanoate, featuring a benzyloxy group attached to the 4-position of the phenyl ring. 4-(benzyloxy)phenyl butanoate is characterized by its ester functional group, which is formed by the reaction of a carboxylic acid and an alcohol. The benzyloxy group provides additional aromatic character and may influence the compound's reactivity and physical properties. 4-(benzyloxy)phenyl butanoate is used in various applications, including as an intermediate in the synthesis of pharmaceuticals and other organic compounds, due to its potential to undergo further chemical transformations. Its structure allows for the exploration of different chemical reactions, such as hydrolysis to remove the benzyl protecting group or other functional group modifications, making it a versatile building block in organic synthesis.

6638-15-9

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6638-15-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6638-15-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6638-15:
(6*6)+(5*6)+(4*3)+(3*8)+(2*1)+(1*5)=109
109 % 10 = 9
So 6638-15-9 is a valid CAS Registry Number.

6638-15-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-phenylmethoxyphenyl) butanoate

1.2 Other means of identification

Product number -
Other names 4-(benzyloxy)phenyl butyrate

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:6638-15-9 SDS

6638-15-9Downstream Products

6638-15-9Relevant academic research and scientific papers

Ring-alkyl connecting group effect on mesogenic properties of p-carborane derivatives and their hydrocarbon analogues

Jankowiak, Aleksandra,Kaszynski, Piotr,Tilford, William R.,Januszko, Adam,Ohta, Kiminori,Nagamine, Takashi,Endo, Yasuyuki

supporting information; experimental part, (2010/07/18)

The effect of the phenyl-alkyl connecting group on mesogenic properties of several series of isostructural compounds containing p-carborane (A and B), bicyclo[2.2.2]octane (C), and benzene (D) was investigated using thermal and optical methods. Results de

THE EFFECT OF CARBONYL CONTAINING SUBSTITUENTS IN THE TERMINAL CHAINS ON MESOMORPHIC PROPERTIES IN AROMATIC ESTERS AND THIOESTERS, 2. ACYLOXY GROUPS ON THE PHENOLIC END

Neubert, Mary E.,Wildman, Patricia J.,Zawaski, Michael J.,Hanlon, Carol A.,Benyo, Theresa L.,Vries, Adriaan De

, p. 111 - 158 (2007/10/02)

The effect of replacing an alkoxy (Y=OR') with acyloxy (Y=OCOR') group on the phenolic end of the esters: on their mesomorphic properties has been studied.These esters were prepared by esterification of 4-acyloxyphenols with the appropriate acid chloride.The phenols were synthesized by acylation of 4-benzyloxyphenol with either an aliphatic acid or acid chloride followed by catalytic hydrogenolysis of the benzyl group.A comparison of the melting and clearing temperatures of these acyloxy esters with the corresponding known alkoxy ones showed small increases in both these temperatures for the acyloxy esters.The same types of mesophases (N, SA, SC, SB) were observed in both series, but the SB was more favored when Y=OCOR'.The SC phase was found to occur in the acyloxy series at chain lengths beyond which it disappeared in the alkoxy series.Comparisons were also made with the mesomorphic properties previously reported for the correponding alkyl and α-keto esters.Some correlation was observed between increasing dipole moments of these substituents and increasing transition temperatures but not in the types of mesophases observed.Fewer mesophases were found when the alkyl chain was attached to the benzene ring through a carbon atom than through an oxygen atom.

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