Detail of "25779-13-9"

CAS Number:
25779-13-9
Name:
(S)-(+)-1-Phenyl-1,2-ethanediol
Molecular Structure:
Formula:
C₈H₁₀O₂
Molecular Weight:
138.16
Synonyms:
1,2-Ethanediol,1-phenyl-, (S)-;1,2-Ethanediol, 1-phenyl-, (S)-(+)- (8CI);(+)-(1S)-1-Phenyl-1,2-ethanediol;(+)-1-Phenyl-1,2-ethanediol;(+)-1-Phenylethylene glycol;(+)-Phenyl glycol;(+)-Phenylethane-1,2-diol;(+)-Phenylethylene glycol;(+)-Styrene glycol;(1S)-1-(Phenyl)ethane-1,2-diol;(2S)-2-Phenylethane-1,2-diol;(S)-(+)-Phenyl-1,2-ethanediol;(S)-1-Phenyl-1,2-ethanediol;(S)-1-Phenyl-2-hydroxyethanol;(S)-Phenylethane-1,2-diol;(S)-Styrene glycol;
Density:
1.17 g/cm³
Melting Point:
64-67 °C(lit.)
Boiling Point:
273.5 °C at 760 mmHg
Flash Point:
145.8 °C
Solubility:
Soluble in water
Appearance:
white to light yellow crystal powder
Hazard Symbols:
Xi, T
Risk Codes:
23/24/25-36/37/38
Safety:
24/25-45-36/37/39-26 Details

Famous Chemical Enterprises

Livzon
Total
Shell
Dupont
Exxonmobil
Akzonobel
Basf
Bayer
BP

Reference

Molecular recognition: Molecular recognition. 18. Complexation of chiral glycols, steroidal polyols, and sugars with a multibenzenoid, achiral host as studied by induced circular dichroism spectroscopy: exciton chirality induction in resorcinol-aldehyde cyclotetramer and its use as a supramolecular probe for the assignments of stereochemistry of chiral guests. Kikuchi, Yasuaki; Kobayashi, Kenji; Aoyama, Yasuhiro (Dep. Ind. Chem., Hachinohe Natl. Coll. Technol., Hachinohe 031, Japan). J. Am. Chem. Soc., 114(4), 1351-8 (English) 1992. CODEN: JACSAT. ISSN: 0002-7863. 25779-13-9 and 3057-04-3 which are cas registry numbers are also used here. DOCUMENT TYPE: Journal CA Section: 33 (Carbohydrates) Section cross-reference(s): 28 Resorcinol-dodecanal cyclotetramer I as an achiral host in chloroform forms H-bonded complexes with a variety of chiral di(poly)ols including steroids and sugars. The complexation processes can be followed very conveniently by the induced CD spectroscopy. The binding consts. as detd. by CD titrn. increase in the order: steroidal monool < acyclic glycols < cyclic glycols and steroidal diols < steroidal triol. This order reflects the extent of multiple host-guest H-bonding interactions. All of the resulting complexes exhibit CD with split Cotton effects as a result of exciton chirality induction in otherwise sym. I upon binding of chiral guest. The signs of split Cotton effects for complexes derived from glycols are correlated with the chiralities or abs. configurations of the guests, while those for sugar complexes are governed by the ring conformations (C1 or 1C) of sugar pyranoses. These results suggest that I can be used as a novel, supramol. probe for the assignments of stereochem. of chiral guests. .

An eight-step synthesis of an orally active antihypertensive carba-prostacyclin analog: An eight-step synthesis of an orally active antihypertensive carba-prostacyclin analog. Riefling, B. F.; Radunz, H. E.; Merck, E. (Darmstadt D-6100, Fed. Rep. Ger.). Tetrahedron Lett. 17814-85-6 and 25779-13-9 are cas registry numbers of chemicals which are used as reagents here., 24(49), 5487-90 (English) 1983. CODEN: TELEAY. ISSN: 0040-4039. DOCUMENT TYPE: Journal CA Section: 26 (Biomolecules and Their Synthetic Analogs) Section cross-reference(s): 1 Carbapentanorthia-PGI2 deriv. I was prepd. in eight steps with >5% overall yield from bicycloheptanone II and (+)-PhCH(OH)CH2SH, and shown to have antihypertensive activity in dogs. .

Detail of "25779-13-9"

(S)-(+)-1-Phenyl-1,2-ethanediol

Famous Chemical Enterprises

Related products

Other Products

Supplier Location

Business Type

Certificates

CAS No.25779-13-9 (S)-(+)-1-Phenyl-1,2-ethanediol

CAS No.25779-13-9 (S)-(+)-1-Phenyl-1,2-ethanediol

CAS No.25779-13-9 (S)-(+)-1-Phenyl-1,2-ethanediol

CAS No.25779-13-9 (S)-(+)-1-Phenyl-1,2-ethanediol

CAS No.25779-13-9 (S)-(+)-1-Phenyl-1,2-ethanediol

CAS No.25779-13-9 (S)-(+)-1-Phenyl-1,2-ethanediol

CAS No.25779-13-9 (S)-(+)-1-Phenyl-1,2-ethanediol

CAS No.25779-13-9 (S)-(+)-1-Phenyl-1,2-ethanediol

CAS No.25779-13-9 (S)-(+)-1-Phenyl-1,2-ethanediol

CAS No.25779-13-9 (S)-(+)-1-Phenyl-1,2-ethanediol

CAS No.25779-13-9 (S)-(+)-1-Phenyl-1,2-ethanediol

CAS No.25779-13-9 (S)-(+)-1-Phenyl-1,2-ethanediol

CAS No.25779-13-9 (S)-(+)-1-Phenyl-1,2-ethanediol

CAS No.25779-13-9 (S)-(+)-1-Phenyl-1,2-ethanediol

CAS No.25779-13-9 (S)-(+)-1-Phenyl-1,2-ethanediol

CAS No.25779-13-9 (S)-(+)-1-Phenyl-1,2-ethanediol

CAS No.25779-13-9 (S)-(+)-1-Phenyl-1,2-ethanediol

CAS No.25779-13-9 (S)-(+)-1-Phenyl-1,2-ethanediol

CAS No.25779-13-9 (S)-(+)-1-Phenyl-1,2-ethanediol

CAS No.25779-13-9 (S)-(+)-1-Phenyl-1,2-ethanediol

CAS No.25779-13-9 (S)-(+)-1-Phenyl-1,2-ethanediol

CAS No.25779-13-9 (S)-(+)-1-Phenyl-1,2-ethanediol

Reference