추천 제품
분석
98%
광학 활성
[α]25/D −13°, c = 4 in carbon tetrachloride
bp
218-220 °C/19 mmHg (lit.)
mp
95-100 °C (lit.)
SMILES string
CC1(C)CCC[C@@]2(C)[C@H]1CC[C@@](C)(O)[C@@H]2CC[C@@](C)(O)C=C
InChI
1S/C20H36O2/c1-7-18(4,21)13-9-16-19(5)12-8-11-17(2,3)15(19)10-14-20(16,6)22/h7,15-16,21-22H,1,8-14H2,2-6H3/t15-,16+,18-,19-,20+/m0/s1
InChI key
XVULBTBTFGYVRC-HHUCQEJWSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
Sclareol, a diterpene compound with a labdane skeleton, is mainly used as a raw material in the fragrance industry. It shows potent cytotoxic and cytostatic effect in human leukemic cell lines.
애플리케이션
Sclareol may be used as a starting material in the synthesis of ambergris fragrance chemicals such as ambraoxide, ambrox, methylambraoxide, ambracetal, ambraketal and epiambraketal. It may also be used in the synthesis of (+)-galanolactone, (-)-8-epi-galanolactone and (+)-labdienedial.
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
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.
이미 열람한 고객
The effect of sclareol on growth and cell cycle progression of human leukemic cell lines.
Leukemia Research, 23(3), 217-234 (1999)
Synthesis of ambergris fragrance chemicals from sclareol, involving palladium catalysed key steps.
Tetrahedron Letters, 29(9), 1017-1020 (1988)
Conversion of sclareol into (+)-galanolactone and (+)-labdienedial.
Tetrahedron Letters, 38(16), 2871-2874 (1997)
Discovery and functional characterization of two diterpene synthases for sclareol biosynthesis in Salvia sclarea (L.) and their relevance for perfume manufacture.
BMC plant biology, 12(1), 119-119 (2012)
A short efficient synthesis of ambraketal (four steps) and epiambraketal (five steps) from Sclareol.
Tetrahedron Letters, 35(1), 97-98 (1994)
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