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10034-09-0

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10034-09-0 Usage

General Description

1,3-Butadiene,1-methoxy-, (1E)- is a chemical compound with the molecular formula C5H8O. It is a colorless liquid with a sweet, fruity odor commonly used as a solvent and in the production of various chemicals. 1,3-Butadiene,1-methoxy-, (1E)- is also known as ethyl vinyl ether and is used in the manufacturing of surfactants, resins, and plastics. It is important to note that exposure to 1,3-Butadiene,1-methoxy-, (1E)- can be harmful, as it is considered a potential carcinogen and may cause irritation to the respiratory system and skin. Therefore, proper safety precautions should be taken when handling this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 10034-09-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,3 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10034-09:
(7*1)+(6*0)+(5*0)+(4*3)+(3*4)+(2*0)+(1*9)=40
40 % 10 = 0
So 10034-09-0 is a valid CAS Registry Number.

10034-09-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methoxy-1,3-butadiene

1.2 Other means of identification

Product number -
Other names 1-methoxy-5,6-dihydro-2H-pyran

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:10034-09-0 SDS

10034-09-0Relevant articles and documents

Benzotriazole: A novel synthetic auxiliary

Katritzky, Alan R.,Rachwal, Stanislaw,Hitchings, Gregory J.

, p. 2683 - 2732 (2007/10/02)

Benzotriazole and aldehydes react reversibly to give addition products: in the presence of amines and other NH-compounds water can be eliminated to form products of type Bt-CHR-NR′R″. The latter are versatile intermediates for the preparation of primary, secondary, and tertiary amines and in the alkylation of hydroxylamines, hydrazines, amides, thioamides, and sulfonamides. Polyfunctional amines and other polyfunctional compounds can also be prepared, and they enable significant extending of Mannich reaction. Similar oxygen compounds Bt-CRR′-OR″ enable new syntheses of ethers and esters. Reactions in which benzotriazole is eliminated rather than substituted open up new pathways to enamines, enol ethers, and nitrones. The methodology is capable of extension to a variety of vinylogous systems including benzenoid and heteroaromatic derivatives. In addition to acting as a versatile leaving group, benzotriazolyl residues activate neighboring CH bonds to proton loss and a variety of such applications is described.

1,3-Dipolar Cycloadditions, 90. Diphenylnitrilimine and Substituted Butadienes; Substituent Effects and Rate of Cycloaddition

Fliege, Werner,Huisgen, Rolf,Kolbeck, Winfried,Weberndoerfer, Volkmar

, p. 3438 - 3460 (2007/10/02)

1-Substitued butadienes accept diphenylnitrilimine (2) not at the 1,2- but rather at the 3,4-double bond; the regiospecific cycloaddition furnishes 5-substituted 1,3-diphenyl-2-pyrazolines.The relative addition rates, measured in competition experiments,

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