87877-11-0

Basic information

• Product Name: Benzenepropanoyl chloride, a-amino-, (S)-
• CAS NO: 87877-11-0
• Molecular Formula: C9H10ClNO
• Molecular Weight: 183.637
• Mol File: 87877-11-0.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Benzenepropanoyl chloride, a-amino-, (S)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanoyl chloride, a-amino-, (S)-(87877-11-0)
• EPA Substance Registry System: Benzenepropanoyl chloride, a-amino-, (S)-(87877-11-0)

Safety Data

• Hazardous Substances Data: 87877-11-0(Hazardous Substances Data)

Upstream product

• 63-91-2 L-phenylalanine 

Downstream Products

• 3081-24-1 H-Phe-OEt 
• 7524-50-7 methyl (2S)-2-amino-3-phenylpropanoate hydrochloride 
• 625842-79-7 (+)-methyl ((trifluoromethyl)sulfonyl)-L-phenylalaninate 
• 159090-55-8 N-Boc-N-methyl-L-phenylalanine ethyl ester 
• 4522-04-7 ethyl N-{[(1,1-dimethylethyl)oxy]carbonyl}-L-phenylalaninate 
• 105469-00-9 (S)-N¹-methyl-3-phenylpropane-1,2-diamine 
• 152899-14-4 <3(2'S),4S>-3-(2-Methyl-1-oxooctyl)-4-(phenylmethyl)-2-oxazolidinone 
• 152899-13-3 (4S)-4-benzyl-3-octanoyl-1,3-oxazolidin-2-one 
• 90719-32-7 (S)-4-Benzyl-2-oxazolidinone 
• 3182-95-4 L-Phenylalaninol 
• 2577-90-4 methyl (2S)-2-amino-3-phenylpropanoate 
• 79868-78-3 (S)-(-)-2-amino-1,1,3-triphenyl-1-propanol 
• 35373-92-3 L-phenylalanine methylamide 

Relevant articles and documents

A selective separation of amino acid functionalized ion liquid, preparation method and its application

The invention discloses a functionalized ionic liquid for modifying lipase, the structure of the functionalized ionic liquid is shown as formula (I), wherein M is 1 ~ 2; R1 and R2 are independently selected from substituted or unsubstituted alkyl, and the

Chiral primary-tertiary diamine catalysts derived from natural amino acids for syn-aldol reactions of hydroxy ketones

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Quantitative structure-activity relationships of pine weevil antifeedants, a multivariate approach

Antifeedant activity of mainly phenylpropanoic, cinnamic, and benzoic acids esters was tested on the pine weevil, Hylobius abietis (L.). Of 105 compounds screened for activity, 9 phenylpropanoates, 3 cinnamates, and 4 benzoates were found to be highly active antifeedants. To understand the structure-activity relationships of these compounds, a multivariate analysis study was performed. A number of molecular and substituent descriptors were calculated and correlated to results from two-choice feeding tests with H. abietis. Three local models were developed that had good internal predictive ability. External test sets showed moderate predictivity. In general, low polarity, small size, and high lipophilicity were characteristics for compounds having good antifeedant activity.