(S)-(+)-2-(Dibenzylamino)-3-phenyl-1-propanol

Modify Date: 2024-01-16 18:04:19

(S)-(+)-2-(Dibenzylamino)-3-phenyl-1-propanol Structure
(S)-(+)-2-(Dibenzylamino)-3-phenyl-1-propanol structure
Common Name (S)-(+)-2-(Dibenzylamino)-3-phenyl-1-propanol
CAS Number 111060-52-7 Molecular Weight 331.45100
Density 1.111g/cm3 Boiling Point 488ºC at 760mmHg
Molecular Formula C23H25NO Melting Point 72-74 °C(lit.)
MSDS Chinese USA Flash Point 191.3ºC
Symbol GHS07
GHS07
Signal Word Warning

 Names

Name (s)-(+)-2-dibenzylamino-3-phenyl-1-propanol
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.111g/cm3
Boiling Point 488ºC at 760mmHg
Melting Point 72-74 °C(lit.)
Molecular Formula C23H25NO
Molecular Weight 331.45100
Flash Point 191.3ºC
Exact Mass 331.19400
PSA 23.47000
LogP 4.29240
Vapour Pressure 2.45E-10mmHg at 25°C
Index of Refraction 1.613

 Safety Information

Symbol GHS07
GHS07
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
Risk Phrases R36/37/38
Safety Phrases S26-S36
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2922199090

 Synthetic Route

 Customs

HS Code 2922199090
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%

 Articles6

More Articles
Preparation of Aminoalkyl Chlorohydrin Hydrochlorides: Key Building Blocks for Hydroxyethylamine-Based HIV Protease Inhibitors.

J. Org. Chem. 61 , 3635, (1996)

Enantiomerically pure N,N-dibenzyl-alpha-amino aldehydes reacted with (chloromethyl)lithium, generated in situ from bromochloromethane and lithium metal, to give predominantly erythro aminoalkyl epoxi...

Stereoselective Synthesis of HIV-1 Protease Inhibitor, DMP 323.

J. Org. Chem. 61 , 444, (1996)

DMP 323, a potent HIV-1 protease inhibitor, has been synthesized by an efficient stereoselective process, amenable to large scale preparations. The core C(2) symmetric diol was synthesized by a stereo...

Cyclic HIV protease inhibitors: synthesis, conformational analysis, P2/P2' structure-activity relationship, and molecular recognition of cyclic ureas.

J. Med. Chem. 39 , 3514, (1996)

High-resolution X-ray structures of the complexes of HIV-1 protease (HIV-1PR) with peptidomimetic inhibitors reveal the presence of a structural water molecule which is hydrogen bonded to both the mob...

 Synonyms

(2S)-2-(dibenzylamino)-3-phenylpropan-1-ol
MFCD00191984