129647-37-6 Usage
Description
2-PHTHALIMIDOLACTOSAMINE, HEPTAACETATE (MIXTURE OF ISOMERS) is a light yellow crystalline solid compound with the CAS number 129647-37-6. It is primarily used in organic synthesis and is known for its unique chemical properties that make it a valuable component in various chemical reactions and processes.
Uses
Used in Organic Synthesis:
2-PHTHALIMIDOLACTOSAMINE, HEPTAACETATE (MIXTURE OF ISOMERS) is used as a synthetic building block for the creation of various complex organic molecules. Its unique structure and reactivity allow it to be employed in the synthesis of a wide range of compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-PHTHALIMIDOLACTOSAMINE, HEPTAACETATE (MIXTURE OF ISOMERS) is used as an intermediate in the development of new drugs. Its versatile chemical properties enable it to be incorporated into the molecular structures of potential therapeutic agents, contributing to the discovery of novel medications with improved efficacy and safety profiles.
Used in Agrochemical Industry:
2-PHTHALIMIDOLACTOSAMINE, HEPTAACETATE (MIXTURE OF ISOMERS) is also utilized in the agrochemical industry for the synthesis of new pesticides and other crop protection agents. Its unique chemical properties can be harnessed to create innovative compounds that offer enhanced control of pests and diseases, ultimately contributing to increased crop yields and food security.
Used in Research and Development:
In the field of research and development, 2-PHTHALIMIDOLACTOSAMINE, HEPTAACETATE (MIXTURE OF ISOMERS) serves as a valuable tool for scientists and researchers. Its unique properties make it an ideal candidate for exploring new reaction pathways, understanding the mechanisms of complex chemical processes, and developing new methodologies for organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 129647-37-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,6,4 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 129647-37:
(8*1)+(7*2)+(6*9)+(5*6)+(4*4)+(3*7)+(2*3)+(1*7)=156
156 % 10 = 6
So 129647-37-6 is a valid CAS Registry Number.
129647-37-6Relevant articles and documents
Rapid access to an orthogonally protected Lewis X derivative: An important building block for synthesis of Lewis antigens
Ohmae, Masashi,Takada, Junko,Murakami, Hiroaki,Kimura, -Shunsaku
, p. 438 - 439 (2011)
A novel Lewis X derivative of 1 with an orthogonal set of protecting groups was systematically prepared. Efficient use of the protecting groups for the amino and the hydroxy groups in lactosamine enabled formation of the diol derivative at C3 and C2'. Glycosidation of 1-thio-L-fucoside donor with the diol derivative progressed preferably at the C3 hydroxy group, resulting in prior production of 1. Compound 1 is a key building block toward easy assemblies of Lewis X-related carbohydrate epitopes.
Syntheses of linear tetra-, hexa-, and octa-saccharide fragments of the i-blood group active poly-(N-acetyl-lactosamine) series. Blockwise methods for the synthesis of repetitive oligosaccharide sequences.
Alais,Veyrieres
, p. 11 - 31 (2007/10/02)
N-Phthaloylation of lactosamine gave various glycosyl donors (beta-chloride, beta-trichloroacetimidate) and glycosyl acceptors (3',4'-diol). Coupling of the chloride with a methyl beta-D-glycoside led to the tetrasaccharide fragment, beta-D-Galp-(1----4)-
