1875-87-2 Usage
Uses
Used in Fragrance Industry:
2,5-Dichlorophenethyl alcohol is used as a fragrance agent for its strong herbal, floral scent, enhancing the aroma profiles of personal care products and perfumes.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2,5-Dichlorophenethyl alcohol is utilized as an intermediate in the synthesis of various organic compounds, contributing to the development of new medications and therapeutic agents.
Used in Chemical Synthesis:
2,5-Dichlorophenethyl alcohol is employed as a key intermediate in the synthesis of a range of organic compounds, facilitating the creation of diverse chemical products for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1875-87-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,7 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1875-87:
(6*1)+(5*8)+(4*7)+(3*5)+(2*8)+(1*7)=112
112 % 10 = 2
So 1875-87-2 is a valid CAS Registry Number.
1875-87-2Relevant articles and documents
Solution and Flash Vacuum Pyrolysis of Some 2,6-Disubstituted β-Phenethylsulfonyl Azides and of β-Styrenesulfonyl Azide
Abramovitch, Rudolph A.,Kress, Albert O.,Pillay, Kutten S.,Thompson, W. Marshall
, p. 2066 - 2073 (2007/10/02)
Solution thermolysis of 2,6-dichloro-β-phenethyl- and 2,6-dimethyl-β-phenethylsulfonyl azide leads to the formation of the corresponding 5,8-disubstituted 3,4-dihydro-2,1-benzothiazine 2,2-dioxides resulting from a 1,2-chlorine and -methyl shift, respectively, in the intermediates.No insertion into the phenethyl side chain, or into the side-chain methyl group in the 2,6-dimethyl case, was detected.Attempted cyclization of ethene-sulfonanilides to 2,1-benzothiazine 2,2-dioxide failed.The orientation of the dichlorosultam was established unambiguously by its FVP to 4,7-dichloroindoline and by the synthesis of an authentic sample.Solution thermolysis of β-styrenesulfonyl azide gave only hydrogen abstraction (32) and solvent insertion (33) products, but FVP gave indole, phenylacetonitrile, and phenylacetylene.
