모든 사진(3)
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1 G
₩75,212
5 G
₩131,240
About This Item
Linear Formula:
C6H8(=O)2
CAS Number:
Molecular Weight:
112.13
Beilstein:
507419
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
Quality Level
분석
97%
양식
solid
bp
193-195 °C (lit.)
mp
34-38 °C (lit.)
저장 온도
2-8°C
SMILES string
O=C1CCCCC1=O
InChI
1S/C6H8O2/c7-5-3-1-2-4-6(5)8/h1-4H2
InChI key
OILAIQUEIWYQPH-UHFFFAOYSA-N
유전자 정보
human ... ACHE(43) , BCHE(590) , CES1(1066)
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Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
No data available
Flash Point (°C)
No data available
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
이미 열람한 고객
D Scott Wilbur et al.
Bioconjugate chemistry, 13(3), 611-620 (2002-05-16)
Recombinant streptavidin (rSAv) is of interest as a carrier of alpha-emitting radionuclides in pretargeting protocols for cancer therapy. Due to the inherently high kidney localization of rSAv, modification of this protein is required before it can be useful in pretargeting.
C Cervenanský et al.
European journal of biochemistry, 229(1), 270-275 (1995-04-01)
The West African green mamba, Dendroaspis angusticeps, has two toxins, fasciculins, that are non-competitive inhibitors of acetylcholinesterase. Arginine residues of fasciculin 2 were modified with 1,2-cyclohexanedione. Two of these residues, Arg24 and Arg37, reacted very slowly or not at all.
Alma Steinbach et al.
The FEBS journal, 279(7), 1209-1219 (2012-02-09)
The thiamine diphosphate (ThDP) dependent flavoenzyme cyclohexane-1,2-dione hydrolase (CDH) (EC 3.7.1.11) catalyses a key step of a novel anaerobic degradation pathway for alicyclic alcohols by converting cyclohexane-1,2-dione (CDO) to 6-oxohexanoate and further to adipate using NAD(+) as electron acceptor. To
S Adak et al.
The Biochemical journal, 314 ( Pt 3), 985-991 (1996-03-15)
The plausible role of arginine and tyrosine residues at the active side of horseradish peroxidase (HRP) in aromatic donor (guaiacol) oxidation was probed by chemical modification followed by characterization of the modified enzyme. The arginine-specific reagents phenylglyoxal (PGO), 2,3-butanedione and
Andres De la Rossa et al.
Nature neuroscience, 16(2), 193-200 (2013-01-08)
The molecular mechanisms that control how progenitors generate distinct subtypes of neurons, and how undifferentiated neurons acquire their specific identity during corticogenesis, are increasingly understood. However, whether postmitotic neurons can change their identity at late stages of differentiation remains unknown.
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