(r)-(-)-n-benzyl-2-phenylglycinol structure
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Common Name | (r)-(-)-n-benzyl-2-phenylglycinol | ||
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CAS Number | 14231-57-3 | Molecular Weight | 227.30200 | |
Density | 1.1g/cm3 | Boiling Point | 386.4ºC at 760mmHg | |
Molecular Formula | C15H17NO | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | 136.9ºC | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of (r)-(-)-n-benzyl-2-phenylglycinol(R)-(−)-N-Benzyl-2-phenylglycinol is a Glycine (HY-Y0966) derivative[1]. |
Name | (2R)-2-(benzylamino)-2-phenylethanol |
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Synonym | More Synonyms |
Description | (R)-(−)-N-Benzyl-2-phenylglycinol is a Glycine (HY-Y0966) derivative[1]. |
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Related Catalog | |
In Vitro | Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1]. |
References |
Density | 1.1g/cm3 |
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Boiling Point | 386.4ºC at 760mmHg |
Molecular Formula | C15H17NO |
Molecular Weight | 227.30200 |
Flash Point | 136.9ºC |
Exact Mass | 227.13100 |
PSA | 32.26000 |
LogP | 2.90070 |
Vapour Pressure | 0mmHg at 25°C |
Index of Refraction | 1.594 |
Storage condition | 2-8°C |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xi: Irritant; |
Risk Phrases | 36/37/38 |
Safety Phrases | 26-36 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2922199090 |
Precursor 8 | |
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DownStream 7 | |
HS Code | 2922199090 |
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Summary | 2922199090. other amino-alcohols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
Asymmetric Synthesis of alpha-Amino Phosphonic Acids by Diastereoselective Addition of Trimethyl Phosphite onto Chiral Oxazolidines(1).
J. Org. Chem. 61 , 3687, (1996) A simple and general asymmetric synthesis of alpha-amino phosphonic acids is described. The method involves the highly selective addition of trialkyl phosphite onto various chiral oxazolidines. Oxazap... |
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Micouin, L. et al.
Tetrahedron Lett. 35 , 7223, (1994)
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MFCD00674035 |