19095-29-5 Usage
Structure
A complex bicyclic heptane ring with a double bond and an alcohol group
Chlorine Content
Six chlorine atoms attached to the bicyclic ring
Synthetic Compound
Not found in nature, created through chemical synthesis
Uses
Primarily used as an intermediate in the production of other chemicals
Potential Applications
Pharmaceutical, plastics, and agrochemical industries
Environmental and Health Concerns
Requires careful handling and disposal to prevent harmful effects
Molecular Weight
Approximately 322.3 g/mol
Physical State
Likely a solid at room temperature, due to the presence of multiple chlorine atoms
Solubility
Expected to be soluble in organic solvents, such as dichloromethane or acetone, due to its nonpolar nature
Stability
May be sensitive to heat, light, and moisture due to the presence of the double bond and alcohol group
Reactivity
Could potentially react with nucleophiles, electrophiles, or other reactive species, depending on the reaction conditions
Toxicity
Potentially toxic due to its chlorine content and complex structure; further studies would be needed to determine its specific toxicological profile
Disposal
Must be disposed of according to local, national, and international regulations for hazardous chemicals to prevent environmental contamination and health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 19095-29-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,9 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 19095-29:
(7*1)+(6*9)+(5*0)+(4*9)+(3*5)+(2*2)+(1*9)=125
125 % 10 = 5
So 19095-29-5 is a valid CAS Registry Number.
19095-29-5Relevant academic research and scientific papers
ENZYMATIC ACYLATION USING ACID ANHYDRIDES: CRUCIAL REMOVAL OF ACID
Berger, B.,Rabiller, C. G.,Koenigsberger, K.,Faber, K.,Griengl, H.
, p. 541 - 546 (2007/10/02)
An efficient enzymatic resolution of 7,7-disubstituted 1,4,5,6-tetrachlorobicyclohept-5-en-2-ols was accomplished by means of lipase AY-30 from Candida cylindracea in toluene.When acid anhydrides were used as acyl donors, the enantioselectivity was found to depend strongly on the reaction conditions: Whereas low selectivity (E 200).Alternatively, adsorption of the biocatalyst onto Celite was equally effective (E >300).Complete specificity was obtained when vinyl acetate was used as acyl donor (E ca.1000).
