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Merck
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문서

480819

Sigma-Aldrich

(R)-(+)-Glycidol

97%, optical purity ee: 98% (GLC)

동의어(들):

(R)-(+)-Oxirane-2-methanol

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About This Item

실험식(Hill 표기법):
C3H6O2
CAS Number:
57044-25-4
Molecular Weight:
74.08
Beilstein:
79782
EC Number:
404-660-4
MDL number:
MFCD00074873
UNSPSC 코드:
12352005
PubChem Substance ID:
24871720
NACRES:
NA.22

분석

97%

광학 활성

[α]23/D +15°, neat

광학 순도

ee: 98% (GLC)

불순물

<3% dichloromethane

refractive index

n20/D 1.43 (lit.)

bp

56-57 °C/11 mmHg (lit.)

density

1.116 g/mL at 20 °C (lit.)

저장 온도

−20°C

SMILES string

OC[C@@H]1CO1

InChI

1S/C3H6O2/c4-1-3-2-5-3/h3-4H,1-2H2/t3-/m1/s1

InChI key

CTKINSOISVBQLD-GSVOUGTGSA-N

유사한 제품을 찾으십니까? 방문 제품 비교 안내

일반 설명

Enantioselective esterification of (R)-(+)-glycidol with n-butyric acid in organic media using hybrid gel-entrapped lipase on Celite has been reported.

애플리케이션

(R)-(+)-Glycidol may be used in the following synthesis:
  • heteroarylpropane-2,3-diols, useful for combinatorial oligomer synthesis
  • enantiomerically pure (2S,3S)- and (2S,3R)-threoninol and -hydroxyphenylalaninol
  • 2-amino-1,4-anhydro-pentitol and 3-amino-1,5-anhydro-4-deoxy-hexitol with the arabino configuration
  • (S)-4-tosyloxymethyl-2-oxazolidinone, required for the synthesis of protected amino alcohol derivatives
  • 1-(S)-[3-hydroxy-2-(phosphonomethoxy)propyl]cytosine [(S)-HPMPC]
  • chiral building block used to construct an epoxyvinyl iodide intermediate in a synthesis of a furanocembrane, a marine natural product

신호어

Danger

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Carc. 1B - Eye Dam. 1 - Muta. 2 - Repr. 1B - Self-react. C - Skin Corr. 1B - STOT SE 3

표적 기관

Respiratory system

Storage Class Code

5.2 - Organic peroxides and self-reacting hazardous materials

WGK

WGK 3

Flash Point (°F)

161.6 °F

Flash Point (°C)

72 °C

개인 보호 장비

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

시험 성적서(COA)

제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.

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문서 라이브러리 방문

Tetrahedron Letters, 47, 6401-6401 (2006)
A New Route for Protected Amino Alcohols from (R)-Glycidol. Copper (I) Mediated Alkylation of 4-Tosyloxymethyl-2-oxazolidinone.
Iwama S and Katsumura S.
Bulletin of the Chemical Society of Japan, 67(12), 3363-3365 (1994)
Synthesis of propane-2, 3-diol combinatorial monomers.
Acevedo OL and Andrews RS.
Tetrahedron Letters, 37(23), 3931-3934 (1996)
N Frank et al.
Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment, 30(1), 69-79 (2012-10-23)
Glycidyl esters (GEs) are known to be formed during vegetable oil processing. Because of their structure, it has been hypothesised that GEs, like fatty acid esters of chloropropanols (MCPD esters), may be accepted as substrates by gut lipases to release
Hiroshi Honda et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 49(10), 2536-2540 (2011-07-12)
Hemoglobin (Hb) adducts are frequently used to address and/or monitor exposure to reactive chemicals. Glycidol (G), a known animal carcinogen, has been reported to form Hb adducts. Here, we measure G adduct levels in humans who daily ingest DAG oil
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