88376-47-0 Usage
Explanation
The full chemical name of the compound, indicating its structure and stereochemistry.
Explanation
The primary applications of the compound in the industry, highlighting its versatility.
Explanation
The appearance and odor of the compound, which are important for handling and safety.
Explanation
The compound's solubility properties, which determine its compatibility with other substances and its use in various applications.
Explanation
The compound's stability, which is crucial for its safe handling and storage.
Explanation
The compound's potential reactivity, which is important for understanding its limitations and safety precautions.
Explanation
The compound's hazard classification, which indicates the potential risks associated with its use and exposure.
Explanation
The potential health effects of exposure to the compound, which are important for safety and proper handling procedures.
Common Uses
Plasticizer in PVC production, solvent in paints, coatings, and adhesives
Physical State
Colorless, odorless liquid
Solubility
Insoluble in water, soluble in organic solvents
Stability
Relatively stable under normal conditions
Reactivity
Can react with strong oxidizing agents
Hazard Classification
Classified as a hazardous substance
Health Effects
Can cause irritation to skin, eyes, and respiratory system
Check Digit Verification of cas no
The CAS Registry Mumber 88376-47-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,3,7 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 88376-47:
(7*8)+(6*8)+(5*3)+(4*7)+(3*6)+(2*4)+(1*7)=180
180 % 10 = 0
So 88376-47-0 is a valid CAS Registry Number.
88376-47-0Relevant academic research and scientific papers
Crout, David H.G.,Morrey, Stephen M.
, p. 2435 - 2440 (1983)
Two synthetic routes to the enantiomers of acetoin (2) of high optical purity have been devised.One starting from (S)-3-methylbut-3-en-2-ol (9) led to (S)-(+)-acetoin (13).The other, starting from (2R,3R)-butane-2,3-diol gave (R)-(-)-acetoin (16).
Acetoin Metabolism: Stereochemistry of the Acetoin Produced by the Pyruvate Decarboxylase of Wheat Germ and by the α-Acetolactate Decarboxylase of Klebsiella aerogenes
Crout, David H. G.,Littlechild, Jennifer,Morrey, Stephen M.
, p. 105 - 108 (2007/10/02)
Acetoin (3-hydroxybutan-2-one) (1) produced from pyruvate and acetaldehyde by the pyruvate decarboxylase of wheat germ consists of a mixture of enantiomers with the (S)-(+)-isomer preponderating.With pyruvate alone as substrate, racemic acetoin is produce
