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L-Pro-ol

Names

[ CAS No. ]:
23356-96-9

[ Name ]:
L-Pro-ol

[Synonym ]:
2-Pyrrolidinemethanol
EINECS 245-605-2
H-L-PRO-OL
MFCD00005255
(S)-(+)-Prolinol
2-Pyrrolidinylmethanol
DL-Prolinol
Pyrrolidine, 2-(hydroxymethyl)-
2-Pyrrolidinemethanol, (2S)-
(S)-(+)-2-(Hydroxymethyl)Pyrrolidine
(2S)-pyrrolidin-2-ylmethanol
L-Prolinol
(2S)-2-Pyrrolidinylmethanol
(S)-Pyrrolidin-2-ylmethanol
H-PROLINOL
pyrrolidin-2-ylmethanol
Prolinol
L-Pro-ol
rac-prolinol
(S)-Prolinol
(2S)-2-Pyrrolidinemethanol
(S)-(+)-2-Pyrrolidinemethanol
H-PRO-OL
L(+)-Prolinol
(2S)-prolinol

Chemical & Physical Properties

[ Density]:
1.0±0.1 g/cm3

[ Boiling Point ]:
211.0±0.0 °C at 760 mmHg

[ Molecular Formula ]:
C5H11NO

[ Molecular Weight ]:
101.147

[ Flash Point ]:
86.1±0.0 °C

[ Exact Mass ]:
101.084061

[ PSA ]:
32.26000

[ LogP ]:
-0.67

[ Vapour Pressure ]:
0.0±0.9 mmHg at 25°C

[ Index of Refraction ]:
1.455

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xi:Irritant

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36-S37/39

[ WGK Germany ]:
3

[ HS Code ]:
2933990090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2933990090

[ Summary ]:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Three-dimensional quantitative structure-activity relationship analyses of substrates of the human proton-coupled amino acid transporter 1 (hPAT1).

Bioorg. Med. Chem. 19 , 6409-18, (2011)

The proton-coupled amino acid transporter hPAT1 has recently gained much interest due to its ability to transport small drugs thereby allowing their oral administration. A three-dimensional quantitati...

Chiral Diphenylprolinol TES ether promoted conjugate addition-aldol-dehydration reactions between alpha,beta-unsaturated aldehydes and 2-N-protected amino benzaldehydes.

Org. Lett. 9(6) , 965-8, (2007)

A conjugate addition-aldol-dehydration reaction of alpha,beta-unsaturated aldehydes with 2-N-protected amino benzaldehydes has been developed. The process is promoted by (S)-diphenylprolinol TES ether...

Asymmetric alkynylation of aldehydes with propiolates without high reagent loading and any additives.

Org. Biomol. Chem. 9(12) , 4425-8, (2011)

The asymmetric alkynylation of aliphatic and aromatic aldehydes with propiolates was mediated by dialkylzinc and a novel prolinol catalyst without high reagent loading and any additives, such as Ti(Oi...


More Articles


Related Compounds

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