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35466-87-6

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35466-87-6 Usage

General Description

2,5-DIOXAHEXANEDIOIC ACID DIETHYL ESTER, also known as diethyl 2,5-dioxohexanedioate, is a chemical compound commonly used as a solvent and a reagent in organic synthesis. It is a diester formed from the reaction of diethyl malonate with oxalyl chloride. 2,5-DIOXAHEXANEDIOIC ACID DIETHYL ESTER is a colorless liquid with a fruity odor, and it is flammable and can be harmful if swallowed, inhaled, or comes into contact with the skin. It is commonly used in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Additionally, it is used as a solvent in the production of dyes, perfumes, and other products.

Check Digit Verification of cas no

The CAS Registry Mumber 35466-87-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,4,6 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 35466-87:
(7*3)+(6*5)+(5*4)+(4*6)+(3*6)+(2*8)+(1*7)=136
136 % 10 = 6
So 35466-87-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O6/c1-3-11-7(9)13-5-6-14-8(10)12-4-2/h3-6H2,1-2H3

35466-87-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethoxycarbonyloxyethyl ethyl carbonate

1.2 Other means of identification

Product number -
Other names 2,4-DINITROPHENYL 2-ACETAMIDO-2-DEOXY-B-D-GLUCOPYRANOSIDE

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:35466-87-6 SDS

35466-87-6Relevant articles and documents

THE 1,4,2,3-DIOXADIAZINE RING SYSTEM

Dixon, Dabney K. White,Weiss, Randy H.,Nelson, William M.

, p. 4393 - 4396 (1983)

The 1,4,2,3-dioxadiazine ring has been synthesized by oxidation of the corresponding 1,2-bishydroxylamine.When the nitrogen substituents are carbalkoxy groups, thermolysis gives the biscarbonate.

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