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17373-84-1

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17373-84-1 Usage

Preparation

It can be prepared by passing vapors of ethyl butyl oxaloacetate over coke or pumice at 350°C.

Aroma threshold values

Aroma characteristics at 1.0%: sweet fruity with an oily apple-like nuance.

Taste threshold values

Taste characteristics at 10 ppm: fruity, sweet, faintly woody with a drying mouthfeel

Check Digit Verification of cas no

The CAS Registry Mumber 17373-84-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,7 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17373-84:
(7*1)+(6*7)+(5*3)+(4*7)+(3*3)+(2*8)+(1*4)=121
121 % 10 = 1
So 17373-84-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O4/c1-3-5-6-13-9(11)7-8(10)12-4-2/h3-7H2,1-2H3

17373-84-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-O-butyl 1-O-ethyl propanedioate

1.2 Other means of identification

Product number -
Other names malonic acid ethyl ester-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:17373-84-1 SDS

17373-84-1Downstream Products

17373-84-1Relevant articles and documents

Efficient synthesis of dissymmetric malonic acid S, O -esters via monoalcoholysis of symmetric dithiomalonates under neutral conditions

Matsuo, Kazumasa,Shindo, Mitsuru

supporting information; experimental part, p. 4406 - 4409 (2011/10/08)

A novel method for the highly selective synthesis of dissymmetric S,O-malonates starting from symmetric diphenyl dithiomalonates under neutral conditions is described. The key step is the thermal formation of an acylketene, the stability of which would co

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