35310-97-5 Usage
Uses
Used in Organic Synthesis:
6,6-Dichlorofulvene is used as a building block in the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of materials, making it a valuable component in the field of organic chemistry.
Used in Material Science:
In the field of material science, 6,6-dichlorofulvene is used as a precursor for the development of new materials. Its properties can be harnessed to produce materials with specific characteristics, such as improved stability or reactivity, which can be beneficial in various applications.
Used in Pharmaceutical Industry:
6,6-Dichlorofulvene is used as an intermediate in the synthesis of pharmaceutical compounds. Its reactivity and structural features make it a useful component in the development of new drugs, potentially leading to advancements in medicine.
Used in Chemical Research:
6,6-Dichlorofulvene is employed as a research tool in chemical studies. Its properties and reactivity can provide insights into the behavior of organochlorine compounds and contribute to a deeper understanding of chemical reactions and processes.
Used in Environmental Applications:
6,6-Dichlorofulvene may be used in environmental applications, such as in the development of new methods for the detection or remediation of pollutants. Its unique properties could potentially be leveraged to create more effective solutions for environmental challenges.
Check Digit Verification of cas no
The CAS Registry Mumber 35310-97-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,3,1 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 35310-97:
(7*3)+(6*5)+(5*3)+(4*1)+(3*0)+(2*9)+(1*7)=95
95 % 10 = 5
So 35310-97-5 is a valid CAS Registry Number.
35310-97-5Relevant articles and documents
Formation and decomposition of chloroaromatic compounds in chlorine-containing benzene/oxygen flames
Burfeindt,Homann
, p. 439 - 447 (2001)
Premixed chlorine-containing, fuel-rich, low-pressure benzene/oxygen flames were analysed for the formation of (oxygenated) chloroaromatic compounds and their radicals by means of the condensation/radical-scavenging method (Hausmann, M., Homann, K.-H., 1995. Ber. Busenges. Phys. Chem. 99, 853-862). Several chlorinated organic compounds (methyl chloride, t-butyl chloride, chlorobenzene, chloroform) were used as additives within a maximum concentration of 10% of total fuel. Product identification and quantification were performed by GC/MS. The extent of formation of chloroaromatic compounds in these flames was largest in the cases of chlorobenzene and chloroform as additives. For chlorobenzene, 12 different chloroaromatics could be analysed in between C7H7Cl and C12H9Cl. Their formation is mainly due to conversion of initial chlorobenzene into substituted or oxidised derivatives, or growth products. Additional chlorination of aromatics is shown to be of minor importance in chlorobenzene-containing flames. Three isomeric (o/m/p) scavenging products could be identified for the chlorophenyl radical. In the chloroform case, 15 chloroaromatics could be analysed in between C6H5Cl and C14H9Cl. The weak C-Cl bond in chloroform is responsible for the high extent of chloroaromatics formation, either by Cl abstraction from the additive or by chlorination reactions via Cl radicals. Additionally, specific pathways to (di)chloroaromatics and chlorinated fulvene-type structures are outlined via CHCl2 and CCl2 radicals.
