H43415
4-羟基-6-甲基-2-吡喃酮
98%
别名:
3,5-二羟基山梨酸 δ-内酯
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关于此项目
经验公式（希尔记法）:
C6H6O3
化学文摘社编号:
分子量:
126.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-619-2
Beilstein/REAXYS Number:
113815
MDL number:
产品名称
4-羟基-6-甲基-2-吡喃酮, 98%
InChI key
NSYSSMYQPLSPOD-UHFFFAOYSA-N
InChI
1S/C6H6O3/c1-4-2-5(7)3-6(8)9-4/h2-3,7H,1H3
SMILES string
CC1=CC(O)=CC(=O)O1
assay
98%
mp
188-190 °C (dec.) (lit.)
Quality Level
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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
Wenjuan Zha et al.
Journal of the American Chemical Society, 126(14), 4534-4535 (2004-04-09)
Metabolic pathway engineering is a powerful tool to synthesize structurally diverse and complex chemicals via genetic manipulation of multistep catalytic systems involved in cell metabolism. Here, we report the rational design of a fatty acid biosynthetic pathway, Brevibacterium ammoniagenes fatty
F Kurosaki
Archives of biochemistry and biophysics, 328(1), 213-217 (1996-04-01)
6-Hydroxymellein synthase is a polyketide biosynthetic enzyme induced in carrot cells which is organized as a homodimer composed of multifunctional subunits. The synthase liberates triacetic acid lactone, instead of 6-hydroxymellein, as a derailment product when the keto-reducing reaction at the
Chiho Taguchi et al.
Acta crystallographica. Section F, Structural biology and crystallization communications, 64(Pt 3), 217-220 (2008-03-08)
Polyketide synthase-1 (PKS-1) is a novel type III polyketide synthase that catalyzes the biosynthesis of hexanoyl triacetic acid lactone in Cannabis sativa (Mexican strain). PKS-1 was overproduced in Escherichia coli, purified and finally crystallized in two different space groups. The
Irreversible inactivation of chicken liver fatty acid synthetase by its substrates acetyl and malonyl CoA. Effect of temperature and NADP n fatty acid and triacetic acid lactone synthesis.
K R Srinivasan et al.
Biochemical and biophysical research communications, 99(3), 920-927 (1981-04-15)
Synthesis of acetoacetyl-CoA by bovine mammary fatty acid synthase.
S Ghayourmanesh et al.
FEBS letters, 132(2), 231-234 (1981-09-28)
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