1077-61-8 Usage
Description
3,4-dihydro-6-methyl-2H-1-benzothiopyran 1,1-dioxide is a heterocyclic chemical compound with the molecular formula C10H10O3S. It is characterized by a benzene ring fused to a thiophene ring and exists as a white solid at room temperature. Known for its strong and unique odor, this compound is recognized for its potential applications in various industries due to its distinct properties.
Uses
Used in the Fragrance Industry:
3,4-dihydro-6-methyl-2H-1-benzothiopyran 1,1-dioxide is used as a scent enhancer for its strong and unique odor, contributing to the creation of various fragrances and perfumes.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 3,4-dihydro-6-methyl-2H-1-benzothiopyran 1,1-dioxide is studied for its potential pharmacological properties, such as anti-inflammatory and antioxidant effects, which may lead to the development of new therapeutic agents.
Used in Pest Control:
3,4-dihydro-6-methyl-2H-1-benzothiopyran 1,1-dioxide has been investigated for its potential role in pest control, with research exploring its use as an insect repellent, offering a possible alternative for managing insect populations in agricultural and residential settings.
Check Digit Verification of cas no
The CAS Registry Mumber 1077-61-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1077-61:
(6*1)+(5*0)+(4*7)+(3*7)+(2*6)+(1*1)=68
68 % 10 = 8
So 1077-61-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O2S/c1-8-4-5-10-9(7-8)3-2-6-13(10,11)12/h4-5,7H,2-3,6H2,1H3
1077-61-8Relevant articles and documents
MODERN FRIEDEL-CRAFTS CHEMISTRY. XI. CYCLIZATION OF ARYL HALOALKYL SULFONES, ARYLSULFONYLACYL CHLORIDES AND THEIR CORRESPONDING SULFIDES
Abdel-Wahab, Aboel-Magd A.,El-Khawaga, Ahmed M.,El-Zohry, Maher F.,Khalaf, Ali A.
, p. 31 - 44 (2007/10/02)
The sulfone group deactivation for cyclialkylation and cycliacylation reactions in the presence of Friedel-Crafts catalysts was demonstrated in a number of aryl chloroalkylsulfones (1-8) and arylsulfonylacyl chlorides (17a-22a), respectively.As expected, the corresponding arylchloroalkyl sulfides (9-16) and arylmercaptoacyl chlorides (13a-28a) underwent ring-closure reaction in most cases under the same conditions.The ease of cyclization was governed by the ring size, the stability of the attacking carbocation and the nucleophilicity of the aryl moiety.Also, the behaviour of benzyl sulfones (29, 31a, and 32a) and sulfides (33, 34a and 36a) was inconsistent.Noteworthy, the Friedel-Crafts cyclization reaction is thus considered an accessible method for the synthesis of compounds 37-41 and 45, 51.
