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88733-72-6

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88733-72-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88733-72-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,7,3 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 88733-72:
(7*8)+(6*8)+(5*7)+(4*3)+(3*3)+(2*7)+(1*2)=176
176 % 10 = 6
So 88733-72-6 is a valid CAS Registry Number.

88733-72-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name benzoic acid,heptan-4-ol

1.2 Other means of identification

Product number -
Other names benzoic acid-(1-propyl-butyl 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:88733-72-6 SDS

88733-72-6Downstream Products

88733-72-6Relevant articles and documents

ACYLATION REACTION OF HYDROXYL GROUP

-

Page/Page column 15-16, (2010/07/03)

Disclosed is a selective ester production process of an alcoholic hydroxyl group, which proceeds under chemically mild conditions, while having adequate environmental suitability, operability and economical efficiency. Specifically disclosed is a process for producing an ester compound, which is characterized in that an alcohol and a carboxylic acid ester compound are reacted in the presence of a compound containing zinc element, thereby selectively acylating a hydroxyl group of the alcohol.

ANOMALOUS ORIENTATION EFFECTS DURING BENZOYLOXYLATIONS BY "SILVER BROMIDE DIBENZOATE"

Bryce-Smith, Derek,Isaacs, Neil S.,Tumi, Seddeg O.

, p. 1471 - 1472 (2007/10/02)

The solid complex formed from bromine and silver benzoate reacts with both arenes and alkenes to form aryl and alkyl benzoates, respectively.Highly unusual substituent effects are observed in the benzoyloxylations of arenes.Electron-withdrawing groups (e.g. -NO2, -CN,-CO-) on the aromatic ring facilitate reaction though directing the attacking reagent exclusively to the meta position.In alkanes, tertiary positions are most prone to attack.

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