14133-35-8 Usage
Uses
Used in Organic Synthesis:
METHYL 3-AMINO-3-DEOXY-ALPHA-D-MANNOPYRANOSIDE HYDROCHLORIDE is used as a synthetic building block for the creation of more complex organic molecules. Its unique structure allows it to be a valuable component in the synthesis of various compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, METHYL 3-AMINO-3-DEOXY-ALPHA-D-MANNOPYRANOSIDE HYDROCHLORIDE is used as a key intermediate in the development of novel drugs. Its unique chemical properties make it a promising candidate for the synthesis of new therapeutic agents, particularly those targeting carbohydrate-related biological processes.
Used in Research and Development:
METHYL 3-AMINO-3-DEOXY-ALPHA-D-MANNOPYRANOSIDE HYDROCHLORIDE is also used as a research tool in academic and industrial laboratories. Its unique structure and reactivity make it an interesting compound for studying various chemical reactions and exploring new synthetic pathways.
Used in Material Science:
In the field of material science, METHYL 3-AMINO-3-DEOXY-ALPHA-D-MANNOPYRANOSIDE HYDROCHLORIDE may find applications in the development of new materials with specific properties, such as improved biocompatibility or enhanced chemical stability. Its unique structure could contribute to the creation of advanced materials for various applications, including medical devices, sensors, and coatings.
Check Digit Verification of cas no
The CAS Registry Mumber 14133-35-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,1,3 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14133-35:
(7*1)+(6*4)+(5*1)+(4*3)+(3*3)+(2*3)+(1*5)=68
68 % 10 = 8
So 14133-35-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H15NO5.ClH/c1-12-7-6(11)4(8)5(10)3(2-9)13-7;/h3-7,9-11H,2,8H2,1H3;1H/t3-,4+,5-,6+,7+;/m1./s1
14133-35-8Relevant academic research and scientific papers
Direct stereocontrolled synthesis of 3-amino-3-deoxy-β- mannopyranosides: Importance of the nitrogen protecting group on stereoselectivity
Crich, David,Xu, Huadong
, p. 5183 - 5192 (2008/02/08)
(Chemical Equation Presented) The highly stereocontrolled synthesis of the 3-amino-3-deoxy-β-mannopyranosides is achieved by means of thioglycoside donors protected with a 4,6-O-benzylidene or alkylidene acetal and a benzylidene imine group. Among the var