00010
Abietic acid
technical, ~75% (GC)
동의어(들):
7,13-abietadien-18-oic acid, Abietate, L-Abietic acid, Rosin acid, Sylvic acid, sylvic acid
로그인조직 및 계약 가격 보기
모든 사진(1)
About This Item
실험식(Hill 표기법):
C20H30O2
CAS Number:
Molecular Weight:
302.45
Beilstein:
2221451
EC Number:
MDL number:
UNSPSC 코드:
12352002
eCl@ss:
32150233
PubChem Substance ID:
NACRES:
NA.22
추천 제품
grade
technical
Quality Level
분석
~75% (GC)
양식
solid
광학 활성
[α]20/D −85±10°, c = 1% in ethanol
mp
139-142 °C (lit.)
150-165 °C
작용기
carboxylic acid
저장 온도
2-8°C
SMILES string
CC(C)C1=CC2=CC[C@@H]3[C@](C)(CCC[C@@]3(C)C(O)=O)[C@H]2CC1
InChI
1S/C20H30O2/c1-13(2)14-6-8-16-15(12-14)7-9-17-19(16,3)10-5-11-20(17,4)18(21)22/h7,12-13,16-17H,5-6,8-11H2,1-4H3,(H,21,22)/t16-,17+,19+,20+/m0/s1
InChI key
RSWGJHLUYNHPMX-ONCXSQPRSA-N
유전자 정보
human ... TNF(7124)
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
Abietic acid can be used as a precursor in the preparation of:
It can also be used as a starting material in the total synthesis of:
- Epoxy and petrochemical curing agents.
- Dehydroabietic acid derivatives as potential antitumor, antimycotic, and antiviral agents.
It can also be used as a starting material in the total synthesis of:
- (−)-triptonide and (−)-triptolide as potent antitumor and immunosuppressant agents
- quinone (−)-12-deoxyroyleanone as antileishmanial agent
- abietic acid-derived catechol (methyl 11,12-dihydroxyabietate-8,11,13-trien-18-oate, MDTO) as a potential antioxidant agent
기타 정보
Starting material for natural product synthesis; Epoxidation with MCPBA
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Aquatic Acute 1 - 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
이미 열람한 고객
G. Buchbauer et al.
Scientia Pharmaceutica, 53, 173-173 (1985)
Synthesis and biological evaluation of dehydroabietic acid derivatives.
Gonzalez M A, et al.
European Journal of Medicinal Chemistry, 45(2), 811-816 (2010)
S. Valverde et al.
Tetrahedron, 42, 573-573 (1986)
H. Okawara et al.
Tetrahedron Letters, 23, 1087-1087 (1982)
Regioselective routes towards 14-hydroxyabietane diterpenes. A formal synthesis of immunosuppressant (−)-triptolide from (+)-abietic acid.
Alvarez-Manzaneda E, et al.
Tetrahedron, 63(45), 11204-11212 (2007)
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