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Merck
모든 사진(1)

문서

A9424

Sigma-Aldrich

Abietic acid

≥65% (GC)

로그인조직 및 계약 가격 보기


About This Item

실험식(Hill 표기법):
C20H30O2
CAS Number:
Molecular Weight:
302.45
Beilstein:
2221451
EC Number:
MDL number:
UNSPSC 코드:
12352000
PubChem Substance ID:

농도

≥65% (GC)

mp

139-142 °C (lit.)

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

교체됨

제품 번호
설명
가격

픽토그램

Exclamation markEnvironment

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


시험 성적서(COA)

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문서 라이브러리 방문

Alan Talevi et al.
Bioorganic & medicinal chemistry letters, 17(6), 1684-1690 (2007-01-20)
Linear discriminant analysis was performed to derive discriminant functions based on 2D descriptors and capable of classifying anticonvulsant from non-anticonvulsant compounds. Through application in virtual screening of the discriminant function which performed best in the validation steps, abietic acid was
Xian-Wen Yang et al.
Bioorganic & medicinal chemistry, 18(2), 744-754 (2009-12-22)
Twenty-five new (abiesadines A-Y, 1-25) and 29 known (26-54) diterpenes were isolated from the aerial parts of Abies georgei. Abiesadine A (1) is a novel 8,14-seco-abietane, while abiesadine B (2) is a novel 9,10-seco-abietane. The structures of the new compounds
Yi He et al.
Journal of pharmaceutical and biomedical analysis, 66, 345-348 (2012-04-10)
An herbal drug for the treatment of psoriasis showed severe clinical adverse reactions. The main component of adulterant was isolated from the drug and its chemical structure was elucidated as abietic acid using NMR, HR-MS, and HPLC-DAD-MS. Although abietic acid
Simon Janocha et al.
Chembiochem : a European journal of chemical biology, 14(4), 467-473 (2013-02-02)
Cytochrome P450s are very versatile enzymes with great potential for biotechnological applications because of their ability to oxidize unactivated CH bonds. CYP105A1 from Streptomyces griseolus was first described as a herbicide-inducible sulfonylurea hydroxylase, but it is also able to convert
Roberto E Di Paolo et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 9(15), 2214-2220 (2008-10-03)
The synthesis and photophysical properties of six new abietic acid based amine end-capped p-phenylenevinylene trimers (AECPV3) in their lowest excited singlet states are presented. The AECPV3 compounds show a large red-shift of both the absorption (25-30 nm) and emission (37-42

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