737000-92-9 Usage
Uses
Used in Pharmaceutical Research:
(S)-(+)-1-CYCLOHEXYLETHYL ISOTHIOCYANATE is used as a key intermediate in the synthesis of various organic compounds for pharmaceutical research. Its unique biological activity makes it a promising candidate for the development of new drugs and therapeutic agents.
Used in Agriculture:
In the agricultural industry, (S)-(+)-1-CYCLOHEXYLETHYL ISOTHIOCYANATE is utilized for its potential applications in pest control and crop protection, thanks to its biological activity.
Used in Materials Science:
(S)-(+)-1-CYCLOHEXYLETHYL ISOTHIOCYANATE is employed in materials science for the development of new materials with specific properties, leveraging its unique chemical structure and characteristics.
Used in the Food Industry:
(S)-(+)-1-CYCLOHEXYLETHYL ISOTHIOCYANATE is studied for its potential as a flavor compound in the food industry, where its unique properties could be harnessed to create novel flavors and enhance the sensory experience of consumers.
Check Digit Verification of cas no
The CAS Registry Mumber 737000-92-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,7,0,0 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 737000-92:
(8*7)+(7*3)+(6*7)+(5*0)+(4*0)+(3*0)+(2*9)+(1*2)=139
139 % 10 = 9
So 737000-92-9 is a valid CAS Registry Number.
737000-92-9Relevant academic research and scientific papers
Asymmetric organocatalysis with novel chiral thiourea derivatives: Bifunctional catalysts for the Strecker and nitro-Michael reactions
Tsogoeva, Svetlana B.,Yalalov, Denis A.,Hateley, Martin J.,Weckbecker, Christoph,Huthmacher, Klaus
, p. 4995 - 5000 (2007/10/03)
Novel bifunctional organocatalysts bearing both a thiourea moiety and an imidazole group on a chiral scaffold were synthesized and applied to the Strecker synthesis and nitro-Michael reaction. The addition of acetone to nitroolefins in the presence of these novel bifunctional organocatalysts gave enantioselectivities (up to 87 % ee) that are superior to those generated by the proline and/or homo-proline tetrazole catalysts described in the literature. Wiley-VCH Verlag GmbH & Co. KGaA, 2005.
