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626-36-8

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626-36-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 626-36-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 626-36:
(5*6)+(4*2)+(3*6)+(2*3)+(1*6)=68
68 % 10 = 8
So 626-36-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H8N2O3/c1-2-9-4(8)6-3(5)7/h2H2,1H3,(H3,5,6,7,8)

626-36-8SDS

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 Ethyl allophanate

1.2 Other means of identification

Product number -
Other names Carbamic acid, (aminocarbonyl)-, ethyl 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:626-36-8 SDS

626-36-8Relevant articles and documents

-

Loeb

, p. 2343 (1886)

-

PROCESS FOR STRAIGHTENING KERATIN FIBRES WITH A HEATING MEANS AND DENATURING AGENTS

-

, (2010/03/02)

The invention relates to a process for straightening keratin fibres, comprising: (i) a step in which a straightening composition containing at least two denaturing agents is applied to the keratin fibres, (ii) a step in which the temperature of the keratin fibres is raised, using a heating means, to a temperature of between 110 and 250° C.

Reactions of trimethylsilyl isocyanate with alcohols and phenols

Pudovik,Krepysheva,Kharitonov,Pudovik

, p. 325 - 326 (2007/10/03)

Mono-and diphenols add to trimethyl isocyanate on heating to give the corresponding aryl urethanes. Ethanol reacts with trimethylsilyl isocyanate to give ethyl urethane and ethyl allophanate in a ratio determined by reaction conditions.

Reactions of N-Sulfinyl Compounds, XV. - Synthesis of 2-Alkenesulfinic Acid Amides - Structure-Reactivity Relationships for N-Sulfinyl Compounds as Enophiles

Bussas, Reinhard,Kresze, Guenter

, p. 545 - 563 (2007/10/02)

The reactivity of N-sulfinyl compounds R6NSO 2 in ene-reactions shows a large variation depending on the nature of the group R6.Haloalkanesulfonamide derivatives react even with very unreactive alkenes.The scope of this method for the synthesis of sulfinic acid amides and the side reactions are discussed.

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