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2-Furancarbonyl chloride, 5-propyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87395-50-4

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87395-50-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87395-50-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,3,9 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 87395-50:
(7*8)+(6*7)+(5*3)+(4*9)+(3*5)+(2*5)+(1*0)=174
174 % 10 = 4
So 87395-50-4 is a valid CAS Registry Number.

87395-50-4SDS

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 5-propylfuran-2-carbonyl chloride

1.2 Other means of identification

Product number -
Other names 5-n-propyl-2-furoyl chloride

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:87395-50-4 SDS

87395-50-4Upstream product

87395-50-4Downstream Products

87395-50-4Relevant academic research and scientific papers

PERMEABLE MEMBRANE/MASS SPECTROMETRIC MEASUREMENT OF AN ENZYMATIC KINETIC ISOTOPE EFFECT: alpha -CHYMOTRYPSIN-CATALYZED TRANSESTERIFICATION.

Calvo,Weisenberger,Anderson,Klapper

, p. 6935 - 6941 (1983)

The **1**6O/**1**8O kinetic isotope effect (KIE) associated with an alpha -chymotrypsin-catalyzed transesterification was measured by using the technique of permeable membrane/mass spectroscopy. This almost in situ method is based upon the ability of the ester product, but not water and other polar compounds, to permeate through a dimethyl silicone membrane, which separates the aqueous reaction solution from the evacuated inlet of the mass spectrometer. The time course of both **1**6O and **1**8O product formation can be followed simultaneously, permitting rapid KIE measurements. With **1**8O-substituted ethanol, the KIE for the formation of both ethyl 2-furoate and ethyl 5-n-propyl-2-furoate from the respective p-nitrophenyl esters is initially normal and decreases with time to reach within approximately 2 min at 25 degree C, pH 8. 5, a constant value of 1. 009 plus or minus 0. 007 for the former and 0. 90 plus or minus 0. 02 for the latter. The large inverse steady-state KIE associated with the formation of ethyl 5-n-propyl-2-furoate decreases when the temperature is raised or when the pH is lowered.

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