모든 사진(1)
About This Item
실험식(Hill 표기법):
C15H13NO2
CAS Number:
Molecular Weight:
239.27
MDL number:
UNSPSC 코드:
12352005
PubChem Substance ID:
NACRES:
NA.22
추천 제품
![5a(R),10b(S)-5a,10b-Dihydro-2-(pentafluorophenyl)-4H,6H-indeno[2,1-b][1,2,4]triazolo[4,3-d][1,4]oxazinium tetrafluoroborate 97%](/deepweb/assets/sigmaaldrich/product/structures/368/775/b5e1517b-14a4-4995-ae5e-98df66198ede/640/b5e1517b-14a4-4995-ae5e-98df66198ede.png)
![(5aR,10bS)-5a,10b-Dihydro-2-(2,4,6-trimethylphenyl)-4H,6H-indeno[2,1-b]-1,2,4-triazolo[4,3-d]-1,4-oxazinium chloride monohydrate 93%](/deepweb/assets/sigmaaldrich/product/structures/104/483/183b49bc-426f-411b-8d11-71bbd4b81022/640/183b49bc-426f-411b-8d11-71bbd4b81022.png)
![1,5,7-Triazabicyclo[4.4.0]dec-5-ene 98%](/deepweb/assets/sigmaaldrich/product/structures/171/446/333d560c-cff6-4958-b489-5acfb3057cce/640/333d560c-cff6-4958-b489-5acfb3057cce.png)
분석
98%
광학 활성
[α]23/D −57±4°, c = 2 in chloroform (or methanol)
mp
227-232 °C (lit.)
작용기
phenyl
SMILES string
O=C1N[C@H]([C@H](O1)c2ccccc2)c3ccccc3
InChI
1S/C15H13NO2/c17-15-16-13(11-7-3-1-4-8-11)14(18-15)12-9-5-2-6-10-12/h1-10,13-14H,(H,16,17)/t13-,14+/m0/s1
InChI key
LTENIVFVXMCOQI-UONOGXRCSA-N
애플리케이션
Versatile chiral auxiliary used in a variety of highly diastereoselective reactions such as Michael additions, Diels-Alder reactions, cyclopropanations, and allylations.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
Davies, I.W. et al.
Tetrahedron Letters, 36, 7619-7619 (1995)
Arun K. Ghosh et al.
The Journal of organic chemistry, 61(18), 6175-6182 (1996-09-06)
Sinefungin (1) a nucleoside antibiotic isolated from Streptomyces has been synthesized from D-ribose. Both the C-6 and C-9 stereogenic centers were constructed by efficient asymmetric syntheses. The C-6 amine stereochemistry was set by a highly diastereoselective allylation (>99% de) of
Akiba, T. et al.
Tetrahedron, 50, 3905-3905 (1994)
Davies, S.G. Sanganee, H.J.
Tetrahedron Asymmetry, 6, 671-671 (1995)
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