204074-52-2

Basic information

• Product Name: (5S)-5,6-Anhydro-2,3,4-trideoxy-2-[[(phenylMethoxy)carbonyl]aMino]-L-glycero-hexonic acid tert-Butyl Ester
• Synonyms: (5S)-5,6-Anhydro-2,3,4-trideoxy-2-[[(phenylMethoxy)carbonyl]aMino]-L-glycero-hexonic acid tert-Butyl Ester
• CAS NO: 204074-52-2
• Molecular Formula: C₁₈H₂₅NO₅
• Molecular Weight: 335.3948
• Product Categories: Amines, Chiral Reagents, Pharmaceuticals, Intermediates & Fine Chemicals
• Mol File: 204074-52-2.mol

Chemical Properties

• Appearance: /
• Solubility: Dichloromethane, Ethyl Acetate
• CAS DataBase Reference: (5S)-5,6-Anhydro-2,3,4-trideoxy-2-[[(phenylMethoxy)carbonyl]aMino]-L-glycero-hexonic acid tert-Butyl Ester(CAS DataBase Reference)
• NIST Chemistry Reference: (5S)-5,6-Anhydro-2,3,4-trideoxy-2-[[(phenylMethoxy)carbonyl]aMino]-L-glycero-hexonic acid tert-Butyl Ester(204074-52-2)
• EPA Substance Registry System: (5S)-5,6-Anhydro-2,3,4-trideoxy-2-[[(phenylMethoxy)carbonyl]aMino]-L-glycero-hexonic acid tert-Butyl Ester(204074-52-2)

Safety Data

• Hazardous Substances Data: 204074-52-2(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
(5S)-5,6-Anhydro-2,3,4-trideoxy-2-[[(phenylMethoxy)carbonyl]aMino]-L-glycero-hexonic acid tert-Butyl Ester is used as a reactant for the production of collagen cross-links, pyridinoline and deoxypyridinoline, which are essential for maintaining the stability and integrity of collagen fibers in the human body. These cross-links are crucial for various applications, including the development of new drugs and therapies targeting connective tissue disorders and other related conditions.
Used in Research and Development:
In the field of research and development, (5S)-5,6-Anhydro-2,3,4-trideoxy-2-[[(phenylMethoxy)carbonyl]aMino]-L-glycero-hexonic acid tert-Butyl Ester serves as a valuable compound for studying the properties and functions of collagen cross-links. This knowledge can be applied to develop innovative treatments and therapies for various medical conditions, such as osteogenesis imperfecta, Ehlers-Danlos syndrome, and other collagen-related disorders.
Used in Cosmetics Industry:
(5S)-5,6-Anhydro-2,3,4-trideoxy-2-[[(phenylMethoxy)carbonyl]aMino]-L-glycero-hexonic acid tert-Butyl Ester may also find applications in the cosmetics industry, where it can be utilized in the development of products aimed at improving skin elasticity, reducing wrinkles, and promoting overall skin health. The compound's role in collagen cross-linking could potentially contribute to the formulation of anti-aging and skin rejuvenation products.

Upstream product

• 112157-39-8 Nα-(Benzyloxycarbonyl)-L-lysine tert-butyl ester 
• 127623-77-2 tert-butyl (S)-2-benzyloxycarbonylamino-6-hydroxyhex-5-enoate 

Downstream Products

• 224629-58-7 (S)-2-benzyloxycarbonylamino-6-bromo-5-oxohexanoic acid tert-butyl ester 
• 309928-91-4 methyl (2S)-2-benzyloxycarbonylamino-6-bromo-5-oxohexanoate 
• 309928-95-8 (2S,5S)-5-azidomethyl-2-benzyloxycarbonylamino-δ-valerolactone 
• 309928-94-7 (2S,5R)-5-azidomethyl-2-benzyloxycarbonylamino-δ-valerolactone 
• 495401-22-4 (2S,5S)-2-benzyloxycarbonylamino-5-bromomethyl-δ-valerolactone 
• 495401-23-5 (2S,5R)-2-benzyloxycarbonylamino-5-bromomethyl-δ-valerolactone 
• 495401-24-6 methyl (2S,5S)-2-benzyloxycarbonylamino-6-bromo-5-hydroxyhexanoate 
• 441353-29-3 allyl (2S,5R)-2-benzyloxycarbonylamino-4-(2-oxiranyl)butanoate 
• 441353-28-2 allyl (2S,5R)-2-benzyloxycarbonylamino-5-hydroxy-6-iodohexanoate 
• 495401-26-8 4-[(S)-2-benzyloxycarbonylamino-2-(tert-butyloxycarbonyl)ethyl]-5-[(S)-3-benzyloxycarbonylamino-3-(tert-butyloxycarbonyl)propyl]-1-[(2R,5S)-5-benzyloxycarbonylamino-5-carboxy-2-hydroxypentyl]-3-pyridiniumolate 
• 495401-25-7 4-[(S)-2-benzyloxycarbonylamino-2-(tert-butyloxycarbonyl)ethyl]-5-[(S)-3-benzyloxycarbonylamino-3-(tert-butyloxycarbonyl)propyl]-1-[(2R,5S)-5-benzyloxycarbonylamino-5-(allyloxycarbonyl)-2-hydroxypentyl]-3-pyridiniumolate 
• 495401-21-3 tert-butyl (2S)-2-benzyloxycarbonylamino-6-bromo-5-hydroxyhexanoate 

Relevant articles and documents

A simple and convenient transformation of L-lysine into pyridinoline and deoxypyridinoline, two collagen cross-links of biochemical interest

Starting from L-lysine as the only chiral building block, pyridinoline and deoxypyridinoline are efficiently synthesised, thus mimicking the postranscriptional formation of these collagen cross-links.