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(S)-(+)-2-(二苄氨基)-1-丙醇

(S)-(+)-2-(二苄氨基)-1-丙醇名称

[ CAS 号 ]:
60479-65-4

[ 中文名 ]:
(S)-(+)-2-(二苄氨基)-1-丙醇

[ 英文名 ]:
(2S)-2-(Dibenzylamino)-1-propanol

[中文别名 ]:

(S)-(+)-2-(二苄基氨基)-1-丙醇

[英文别名 ]:

(S)-2-(N,N-Dibenzylamino)-1-propanol
2-(N,N-dibenzyl)amino-1-propanol
(2S)-2-(Dibenzylamino)-1-propanol
(2S)-2-(dibenzylamino)propan-1-ol
(S)-(+)-2-(Dibenzylamino)-1-propanol
(S)-N,N-dibenzyl-2-amino-1-propanol
S-2-(N,N-dibenzylamino)propanol
(S)-2-(Dibenzylamino)propan-1-ol
N,N-dibenzyl-(S)-2-amino-1-propanol
1-Propanol, 2-[bis(phenylmethyl)amino]-, (2S)-

(S)-(+)-2-(二苄氨基)-1-丙醇物理化学性质

[ 密度 ]:
1.1±0.1 g/cm3

[ 沸点 ]:
374.2±22.0 °C at 760 mmHg

[ 熔点 ]:
46-48ºC(lit.)

[ 分子式 ]:
C₁₇H₂₁NO

[ 分子量 ]:
255.355

[ 闪点 ]:
140.2±18.9 °C

[ 精确质量 ]:
255.162308

[ PSA ]:
23.47000

[ LogP ]:
4.08

[ 蒸汽压 ]:
0.0±0.9 mmHg at 25°C

[ 折射率 ]:
1.583

(S)-(+)-2-(二苄氨基)-1-丙醇MSDS

(S)-(+)-2-(二苄氨基)-1-丙醇安全信息

[ 符号 ]:

GHS07

[ 信号词 ]:
Warning

[ 危害声明 ]:
H315-H319-H335

[ 警示性声明 ]:
P261-P305 + P351 + P338

[ 个人防护装备 ]:
dust mask type N95 (US);Eyeshields;Gloves

[ 危害码 (欧洲) ]:
Xi

[ 风险声明 (欧洲) ]:
36/37/38

[ 安全声明 (欧洲) ]:
26-36

[ 危险品运输编码 ]:
NONH for all modes of transport

[ WGK德国 ]:
3

[ 海关编码 ]:
2922199090

(S)-(+)-2-(二苄氨基)-1-丙醇合成路线

(S)-(+)-2-(二苄氨基)-1-丙醇上下游产品

(S)-(+)-2-(二苄氨基)-1-丙醇上游产品

(S)-(+)-2-(二苄氨基)-1-丙醇下游产品

(S)-(+)-2-(二苄氨基)-1-丙醇海关

[ 海关编码 ]: 2922199090

[ 中文概述 ]:
2922199090. 其他氨基醇及其醚，酯和它们的盐（但含一种以上含氧基的除外）. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:30.0%

[ 申报要素 ]: 品名, 成分含量, 用途, 乙醇胺及其盐应报明色度, 乙醇胺及其盐应报明包装

[ 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%

(S)-(+)-2-(二苄氨基)-1-丙醇文献

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...

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