74774-14-4 Usage
Uses
Used in Pharmaceutical Synthesis:
.beta.-D-Glucopyranose, 1,6-anhydro-6-C-(phenylthio)-, (R)is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure and reactivity enable the development of novel drugs with improved efficacy and reduced side effects.
Used in Biochemical Compounds Synthesis:
In the field of biochemistry, .beta.-D-Glucopyranose, 1,6-anhydro-6-C-(phenylthio)-, (R)serves as a crucial building block for the synthesis of complex biochemical compounds. Its specific stereochemistry allows for the creation of molecules with tailored properties and functions.
Used in Organic Chemistry:
.beta.-D-Glucopyranose, 1,6-anhydro-6-C-(phenylthio)-, (R)is employed as a reagent in organic chemistry, particularly for introducing the phenylthio group at the 6-position of glucose. This modification can lead to the development of new organic compounds with unique properties and potential applications in various industries.
Used in Drug Development:
.beta.-D-Glucopyranose, 1,6-anhydro-6-C-(phenylthio)-, (R)-'s potential applications in drug development make it a valuable asset in the pharmaceutical industry. Its use in the synthesis of novel drugs and its role in introducing specific functional groups can contribute to the discovery of new therapeutic agents with improved pharmacological profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 74774-14-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,7,7 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 74774-14:
(7*7)+(6*4)+(5*7)+(4*7)+(3*4)+(2*1)+(1*4)=154
154 % 10 = 4
So 74774-14-4 is a valid CAS Registry Number.
74774-14-4Relevant academic research and scientific papers
Photobromination of Carbohydrate Derivatives. VI. Funcionalization at C6 of 2,3,4-tri-O-acetyl-1,6-anhydro-β-D-glucopyranose
Ferrier, Robert J.,Furneaux, Richard H.
, p. 1025 - 1036 (2007/10/02)
Photobromination of 2,3,4-tri-O-acetyl-1,6-anhydro-β-D-glucopyranose gives the syrupy 6S (exo) bromide in high yield; further reaction leads to secondary bromination at this position.The monobromide reacts with methanol and thiophenol under conditions of kinetic control to give mainly the endo-methoxy and phenylthio derivatives formed by direct nucleophilic displacement, and from the latter the exo-methoxy acetal was obtained by a second nucleophilic substitution.Acetolysis of these compounds can lead to the coresponding exo-6-acetoxy ester or monocyclicproducts formed by opening of the five-membered rings.
