추천 제품
광학 활성
[α]20/D +14°, c = 1 in pentane
농도
1 M in pentane
bp
35-36 °C
density
0.735 g/mL at 25 °C
저장 온도
−20°C
SMILES string
C[C@@H]1[C@H](C[C@H]2C[C@@H]1C2(C)C)B(CC=C)[C@H]3C[C@H]4C[C@@H]([C@@H]3C)C4(C)C
InChI
1S/C23H39B/c1-8-9-24(20-12-16-10-18(14(20)2)22(16,4)5)21-13-17-11-19(15(21)3)23(17,6)7/h8,14-21H,1,9-13H2,2-7H3/t14-,15-,16+,17+,18-,19-,20-,21-/m0/s1
InChI key
ZIXZBDJFGUIKJS-AXSQLCHVSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
http://www.sigmaaldrich.com/ifb/acta/v35/acta-vol35-2002.html#32
애플리케이션
This allylboration reagent is a convenient, salt-free, stable solution of a chiral allyl borane for asymmetric allylation of aldehydes leading to chiral homoallylic alcohols.
기타 정보
Material may become hazy upon cooler storage, this will not affect use
Under refrigerator storage, these salt-free, Ipc2B(allyl) reagents do not show any appreciable decrease in selectivity is observed after several months. They exhibit excellent reactivity and reactions can be performed at 5°C, even in water.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Aquatic Chronic 2 - Asp. Tox. 1 - Eye Irrit. 2 - Flam. Liq. 1 - Skin Irrit. 2 - STOT SE 3
표적 기관
Central nervous system, Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point (°F)
-56.2 °F
Flash Point (°C)
-49 °C
개인 보호 장비
Eyeshields, Faceshields, Gloves
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.
Total synthesis of epothilones B and D
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Versatile route to 2, 6-dideoxyamino sugars from non-sugar materials: Syntheses of vicenisamine and kedarosamine
Journal of the Chemical Society. Perkin Transactions 1, 1.6, 569-577 (2001)
Synthesis of 16-desmethylepothilone B: improved methodology for the rapid, highly selective and convergent construction of epothilone B and analogues
Chemical Communications (Cambridge, England), 6, 519-520 (1999)
A Concise Stereoselective Total Synthesis of Synargentolide A from 3, 4, 6-Tri-O-acetyl-D-glucal
Synthesis, 2011.08, 1279-1282 (2011)
Total synthesis of (?)-centrolobine: ?-C-glycoside formation via a tandem Grignard addition and stereoselective hemi-ketal reduction
Tetrahedron Letters, 46.12, 2021-2024 (2005)
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