10034-09-0 Usage
Physical state
Colorless liquid
Explanation
Different sources of media describe the Explanation of 10034-09-0 differently. You can refer to the following data:
1. The compound is in a liquid state at room temperature and is colorless, meaning it does not have any visible color.
2. The compound has a pleasant, sweet, and fruity smell, which can be detected by the human nose.
3. 1,3-Butadiene,1-methoxy-, (1E)is commonly used as a solvent, which means it can dissolve other substances. It is also used in the production of various chemicals.
4. The compound is also known by the name ethyl vinyl ether, which is an alternative way to refer to it.
5. The compound is used in the manufacturing of surfactants (substances that reduce the surface tension of a liquid), resins (amorphous, solid substances), and plastics (a wide range of synthetic or semi-synthetic materials).
6. Exposure to 1,3-Butadiene,1-methoxy-, (1E)can be harmful to human health. It is considered a potential carcinogen, which means it may cause cancer. Additionally, it can cause irritation to the respiratory system and skin.
7. Due to the potential health hazards associated with 1,3-Butadiene,1-methoxy-, (1E)-, it is essential to take proper safety precautions when handling this chemical. This may include using personal protective equipment (PPE) such as gloves, goggles, and masks, as well as following proper storage and disposal guidelines.
Odor
Sweet, fruity
Uses
Solvent, production of chemicals
Synonyms
Ethyl vinyl ether
Applications
Surfactants, resins, and plastics
Health hazards
Potential carcinogen, respiratory and skin irritation
Safety precautions
Proper handling and protection
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.
10034-09-0Relevant 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,
