2, 4-Dihydroxyacetophenone

2, 4-Dihydroxyacetophenone

Khoom Taw qhia

2,4-Dihydroxyacetophenone Cov ntaub ntawv yooj yim
Khoom npe: 2, 4-Dihydroxyacetophenone
Synonyms: Resoacetophenone; Resorcinol, 4-acetyl-; 2, 4-Dihydroxyacetoph; NSC 10883; NSC 37559; 4-Acetylresorcinol Resacetophenone; HyMechroMone; IMp. A (EP): 1,3-Dihydroxybenzene (Resorcinol)
CAS: 89-84-9
MF: C8H8O3
MW: 152.15
EINECS: 201-945-3
Khoom Categories: Aromatics; Lwm yam Reagents; Acetophenone Series; Aromatic Acetophenones & Derivatives (substituted); Benzene series; 89-84-9;bc0001;john's
Mol File: 89-84-9.mol
2,4-Dihydroxyacetophenone Structure
 
2,4-Dihydroxyacetophenone Cov Khoom Siv Tshuaj
Melting point 143-144.5 degree (lit.)
Boiling point 234.6 degree (kev kwv yees ntxhib)
ceev 1.18 g / ml ntawm 25 degree (lit.)
Refractive Index 1.4945 (kwv yees)
cia temp. Inert cua, Chav Kub
solubility DMSO (me ntsis), Methanol (me ntsis)
pka ua 7.96 ± 0.18 (Tshaj tawm)
daim ntawv Crystalline hmoov los yog Crystals
xim Tawm-dawb mus rau paj yeeb rau xim av
PH 5 (1g / l, H2O, 20 degree)
rhiab heev Moisture Sensitive
Merck 14,8140
BRN 1282505
InChIKey SULYEHHGGXARJS-UHFFFAOYSA-N
LogP 1.480 (yeem)
CAS DataBase Reference 89-84-9(CAS DataBase Reference)
NIST Chemistry Reference Ethanone, 1-(2, 4-dihydroxyphenyl)-(89-84-9)
EPA Tshuaj Registry System Ethanone, 1-(2, 4-dihydroxyphenyl)- (89-84-9)
 
Cov ntaub ntawv kev nyab xeeb
Hazard Codes Xis
Risk Statements 36/37/38
Cov lus hais txog kev nyab xeeb 26-36-24/25
WGK Germany 2
RTECS ib 7525000
Ceeb toom Irritant
TSCA Yog lawm
HS Code 29145000
 
MSDS Cov Ntaub Ntawv
Tus kws kho mob Lus
Resacetophenone Lus Askiv
SigmaAldrich Lus Askiv
ACROS Lus Askiv
ALFA Lus Askiv
 
2,4-Dihydroxyacetophenone Siv Thiab Synthesis
Chemical Properties 2,4-Dihydroxyacetophenone tshwm li daj-xim av rau reddish-xim av zoo crystalline hmoov. Nws maj mam decomposes hauv dej thiab tuaj yeem yaj hauv dej cawv kub, pyridine, thiab glacial acetic acid. Nyob rau hauv sib piv, nws yog ze li insoluble nyob rau hauv ether, benzene, thiab chloroform. Ib qho tshuaj tiv thaiv nrog hlau chloride ua rau nws txais yuav xim liab.
Siv 2,4-Dihydroxyacetophenone (cas# 89-84-9) yog ib qho khoom siv muaj txiaj ntsig zoo hauv cov organic synthesis. Nws kuj yog siv los ua cov tshuaj nruab nrab rau cov tshuaj. Reagent rau hlau raws li 10% cawv daws. Cov xim liab yog tau nrog ferric ions hauv cov kua qaub me ntsis: Cooper, Ind. Eng. Chem. Qhov quav. Ed. 9, 334 (1937).
Txhais ChEBI: 2',4'-dihydroxyacetophenone yog ib qho dihydroxyacetophenone uas yog acetophenone nqa hydroxy substituents ntawm txoj haujlwm 2' thiab 4'. Nws muaj lub luag haujlwm ua cov nroj tsuag metabolite. Nws yog ib tug tswv cuab ntawm resorcinols thiab dihydroxyacetophenone.
Kev npaj Kev npaj los ntawm cov tshuaj tiv thaiv acetic acid ntawm resorcinol,
nrog zinc chloride (Nencki cov tshuaj tiv thaiv) (94%)
nrog boron trifluoride
nrog Amberlite IR -120 (ib cation txauv resin, sulfonic acid hom) (87%)
nrog polyphosphoric acid (63%)
nrog 70% perchloric acid (33%).
Synthesis Reference (cov) Phau ntawv Journal of the American Chemical Society, 70, p. 428 Ib., 1948DOI:10.1021/j01181a521
Kev ruaj ntseg Profile Muaj tshuaj lom los ntawm kev noj tshuaj. Kev sim ua kom muaj menyuam. Qhov muag mob heev. Thaum rhuab mus rau decomposition nws emissions pa luam yeeb thiab irritating fumes.
Synthesis 2, 4-Dihydroxyacetophenone yog tau los ntawm acetylation ntawm resorcinol thiab acetic acid. Tsis tas li ntawd, nws tseem tuaj yeem tau txais los ntawm reacting resorcinol nrog chloroacetyl lossis acetic anhydride nyob rau hauv muaj zinc chloride.
phiaj Phospholipase (piv txwv li PLA)
 
2,4-Dihydroxyacetophenone Kev Npaj Khoom Siv Thiab Cov Khoom Raw
Cov khoom nyoos Zinc chloride
Cov khoom npaj 7-Hydroxycoumarin-->1-[4-(Benzoyloxy)-2-hydroxyphenyl]-3-phenyl-1,3-propanedione-->1-(2,4-Bis(benzoyloxy)phenyl)ethanone-->7-HYDROXYFLAVONE-->2',4'-DIHYDROXYCHALCONE-->3,7-DIHYDROXYFLAVONE-->4-HYDROXY-7-METHOXYCOUMARIN-->7-HYDROXYFLAVANONE-->ROBINETIN-->4'-Benzyloxy-2'-hydroxyacetophenone-->4-Ethylresorcinol-->4-[3-(2,4-Dimethoxy-3-methylphenyl)propyl]-1,3-benzenediol-->2, 4-Dimethoxyacetophenone

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