A1631
蒽酮
ACS reagent
别名:
9(10H)-蒽酮
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关于此项目
经验公式（希尔记法）:
C14H10O
化学文摘社编号:
分子量:
194.23
EC Number:
201-994-0
UNSPSC Code:
12171500
PubChem Substance ID:
Beilstein/REAXYS Number:
1910173
MDL number:
InChI key
RJGDLRCDCYRQOQ-UHFFFAOYSA-N
InChI
1S/C14H10O/c15-14-12-7-3-1-5-10(12)9-11-6-2-4-8-13(11)14/h1-8H,9H2
SMILES string
O=C1c2ccccc2Cc3ccccc13
grade
ACS reagent
mp
154-157 °C (lit.)
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Application
Used for determination of carbohydrates.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Total synthesis and structure assignment of the anthrone C-glycoside cassialoin.
Yasuhito Koyama et al.
Angewandte Chemie (International ed. in English), 47(6), 1084-1087 (2008-01-01)
Liselotte Krenn et al.
Chemical & pharmaceutical bulletin, 52(4), 391-393 (2004-04-02)
In a study of the anthraderivatives in roots of Rheum emodi, three new anthrone C-glucosides, named 10-hydroxycascaroside C (1), 10-hydroxycascaroside D (2) and 10R-chrysaloin 1-O-beta-D-glucopyranoside (3) were isolated besides the rare compounds cascaroside C (4), cascaroside D (5) and cassialoin
Fredyc Diaz et al.
Journal of natural products, 67(3), 352-356 (2004-03-27)
Cytotoxicity-based, bioassay-guided fractionation of the chloroform-soluble extracts of both the roots and leaves of Picramnia latifolia led to the isolation of two new anthrone C-glycosides, picramniosides G (1) and H (2), two new oxanthrone C-glycosides, mayosides D (3) and E
A microtiter modification of the anthrone-sulfuric acid colorimetric assay for glucose-based carbohydrates.
Alexander Laurentin et al.
Analytical biochemistry, 315(1), 143-145 (2003-04-04)
Jason M Crawford et al.
Nature, 461(7267), 1139-1143 (2009-10-23)
Polyketides are a class of natural products with diverse structures and biological activities. The structural variability of aromatic products of fungal nonreducing, multidomain iterative polyketide synthases (NR-PKS group of IPKSs) results from regiospecific cyclizations of reactive poly-beta-keto intermediates. How poly-beta-keto
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