10289-05-1

Basic information

• Product Name: N-[(1S)-2-Hydro×y-1-benzylethyl]Metho×y carbo×aMide
• Synonyms: N-[(1S)-2-Hydro×y-1-benzylethyl]Metho×y carbo×aMide;(S)-Methyl (1-hydroxy-3-phenylpropan-2-yl)carbamate
• CAS NO: 10289-05-1
• Molecular Formula: C₁₁H₁₅NO₃
• Molecular Weight: 209.2417
• Mol File: 10289-05-1.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: N-[(1S)-2-Hydro×y-1-benzylethyl]Metho×y carbo×aMide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[(1S)-2-Hydro×y-1-benzylethyl]Metho×y carbo×aMide(10289-05-1)
• EPA Substance Registry System: N-[(1S)-2-Hydro×y-1-benzylethyl]Metho×y carbo×aMide(10289-05-1)

Safety Data

• Hazardous Substances Data: 10289-05-1(Hazardous Substances Data)

Usage

General Description

N-[(1S)-2-Hydroxy-1-benzylethyl]Methoxy carbamide is a chemical compound with the molecular formula C12H17NO3. It is an amide derivative with a methoxy group attached to a carbonyl carbon and a hydroxyl group attached to a benzyl ethyl group. N-[(1S)-2-Hydro×y-1-benzylethyl]Metho×y carbo×aMide has potential applications in the pharmaceutical industry due to its ability to modulate biological processes and interact with biological targets. It may be used as a building block in the synthesis of various organic compounds and drugs. Moreover, it might exhibit pharmacological properties that could be beneficial for the treatment of certain medical conditions. Further research and testing are required to fully understand the chemical and biological properties of N-[(1S)-2-Hydroxy-1-benzylethyl]Methoxy carbamide.

Upstream product

• 3182-95-4 L-Phenylalaninol 
• 79-22-1 methyl chloroformate 

Downstream Products

• 209787-89-3 ((S)-2-Phenyl-1-phenylsulfanylmethyl-ethyl)-carbamic acid methyl ester 
• 154659-13-9 (2S,3R,4R)-2--6-methyl-1-phenylheptane-3,4-diol 
• 245107-67-9 N-[(1S)-2-Fluoro-1-benzylethyl]methoxy carboxamide 
• 154659-31-1 (S)-2-methoxycarbonylamino-3-phenylpropanal 

Relevant articles and documents

O-Alkyl S-(Pyridin-2-yl)carbonothiolates: Operationally Simple and Highly Nitrogen-Selective Reagents for Alkoxy Carbonylation of Amino Groups

Amino groups are selectively protected in good yields by reaction with O-Alkyl S-(pyridin-2-yl)carbonothiolates in an appropriate solvent at room temperature in air. Even glucosamine, which contains multiple hydroxyl groups, is selectively N-protected in methanol.

Pinacol cross coupling of 2-[N-(alkoxycarbonyl)amino] aldehydes and aliphatic aldehydes by [V2Cl3(THF)6]2[Zn2Cl 6]. Synthesis of syn,syn-3-[N-(alkoxycarbonyl)amino] 1,2-diols

Slow addition of 2-[N-(alkoxycarbonyl)amino] aldehydes to mixtures of [V2Cl3(THF)6]2[Zn2Cl 6] and aliphatic aldehydes gave syn,syn-3-[N-(alkoxycarbonyl)amino] 1,2-diols in good yield and high enantiomeric purity (>99:1). The alkyl group of the N-alkoxycarbonyl was shown to influence the yield: Me > allyl > Bn > t-Bu. Only the syn,syn diastereomer was observed (>20:1), except with N-Cbz-alaninal (10:1:1), O-benzyl-N-Cbz-serinal (7:1), and N-Cbz-prolinal (5:1 to 12:1). A new serinai derivative, N-Cbz-O-TBS-serinal, was cross coupled with n-pentadecanal to give a derivative of xylo-D-C18-phytosphingosine.