모든 사진(1)
About This Item
실험식(Hill 표기법):
C12H20O6
CAS Number:
Molecular Weight:
260.28
Beilstein:
84382
MDL number:
UNSPSC 코드:
12352201
PubChem Substance ID:
NACRES:
NA.22
추천 제품
Quality Level
분석
97%
양식
solid
광학 활성
[α]20/D +23°, c = 1 in acetone
mp
125-126 °C (dec.) (lit.)
SMILES string
CC1(C)OC[C@@H](O1)[C@H]2OC(O)[C@@H]3OC(C)(C)O[C@@H]23
InChI
1S/C12H20O6/c1-11(2)14-5-6(16-11)7-8-9(10(13)15-7)18-12(3,4)17-8/h6-10,13H,5H2,1-4H3/t6?,7-,8+,9?,10?/m1/s1
InChI key
JWWCLCNPTZHVLF-RGJLLFKYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
Protected mannose intermediate used in the syntheses of ovalicin and of the sugar core of hikizimycin.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
Furstner, A. et al.
Chemistry (Weinheim An Der Bergstrasse, Germany), 12, 76-76 (2006)
Shunya Takahashi et al.
The Journal of organic chemistry, 70(24), 10162-10165 (2005-11-19)
[reaction: see text] A new synthesis of epoxyketone 22 is described that is a key intermediate in Barton's synthesis of ovalicin (2), a powerful anti-angiogenetic inhibitor. The key process for the construction of 22 was ring-closing metathesis of olefins 11
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