ChemicalBook--->CAS DataBase List--->6100-74-9

6100-74-9

6100-74-9 Structure

6100-74-9 Structure
IdentificationBack Directory
[Name]

4-METHOXY-3-HYDROXYACETOPHENONE
[CAS]

6100-74-9
[Synonyms]

NSC 30050
-Hydroxy-4′
Acetoisovanillone
Isoacetovanillone
ACETOISOVANILLONE(SH)
5-Acetyl-2-methoxyphenol
3-HYDROXY-4-METHOXYACETOPHENONE
4-METHOXY-3-HYDROXYACETOPHENONE
4'-METHOXY-3'-HYDROXYACETOPHENONE
3'-Hydroxy-4'-methoxyacetophenone 97%
1-(3-hydroxy-4-methoxy-phenyl)ethanone
1-(3-hydroxy-4-Methoxyphenyl)ethan-1-one
Ethanone, 1-(3-hydroxy-4-Methoxyphenyl)-
[Molecular Formula]

C9H10O3
[MDL Number]

MFCD00182975
[MOL File]

6100-74-9.mol
[Molecular Weight]

166.17
Chemical PropertiesBack Directory
[Appearance]

solid
[Melting point ]

88-92 °C
[Boiling point ]

329.9±27.0 °C(Predicted)
[density ]

1.158
[storage temp. ]

Inert atmosphere,Room Temperature
[solubility ]

DMSO (Slightly), Methanol (Slightly)
[form ]

Solid
[pka]

9.15±0.10(Predicted)
[color ]

Off-White to Yellow
[Stability:]

Stable. Incompatible with strong oxidizing agents.
[InChI]

InChI=1S/C9H10O3/c1-6(10)7-3-4-9(12-2)8(11)5-7/h3-5,11H,1-2H3
[InChIKey]

YLTGFGDODHXMFB-UHFFFAOYSA-N
[SMILES]

C(=O)(C1=CC=C(OC)C(O)=C1)C
[LogP]

1.373 (est)
Hazard InformationBack Directory
[Chemical Properties]

solid
[Uses]

Isoacetovanillone is a volatile compound isolated from oak wood. Also a byproduct in the production of Acetovanillone.
[Definition]

ChEBI: Isoacetovanillone is a member of phenols and a member of methoxybenzenes. It has a role as a metabolite.
[Preparation]

Preparation by saponification of 3-acetoxy-4-methoxy-acetophenone (90%) (59%).
[Synthesis Reference(s)]

Synthetic Communications, 18, p. 1379, 1988 DOI: 10.1080/00397918808078806
[Synthesis]

1-(4-Methoxy-3-propan-2-yloxyphenyl)ethanone

88114-44-7

4-METHOXY-3-HYDROXYACETOPHENONE

6100-74-9

General procedure for the synthesis of 4-methoxy-3-hydroxyacetophenone from 3'-hydroxy-4'-methoxyacetophenone (12): ketone 8 (250 mg, 1.20 mmol) was dissolved in anhydrous CH2Cl2 (3 mL), AlCl3 (208 mg, 1.56 mmol) was added, and the reaction was stirred for 24 h at 18 °C and under nitrogen protection. After completion of the reaction, the mixture was partitioned between water (10 mL) and CH2Cl2 (10 mL). The aqueous phase was extracted once with CH2Cl2 (10 mL), the organic phases were combined, dried with MgSO4, filtered and concentrated under reduced pressure. The light yellow oil obtained was purified by fast chromatography (eluent: ethyl acetate/hexane, 1:4 v/v) to give a white solid 4-methoxy-3-hydroxyacetophenone 124 (172 mg, 86% yield) with a melting point of 88.6-90.5 °C (literature value: 92-93 °C) and a TLC (silica gel plate, unfolding agent: ethyl acetate/hexane, 1:1 v/v) Rf value was 0.4. 1H NMR (300MHz, CDCl3) δ: 7.53-7.56 (m, 2H), 6.89 (d, J=7.5Hz, 1H), 5.73 (br s, 1H), 3.96 (s, 3H), 2.54 (s, 3H).

[storage]

Store at -20°C
[References]

[1] Patent: WO2008/124878, 2008, A1. Location in patent: Page/Page column 38
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
[Hazard Codes ]

Xn
[Risk Statements ]

22
[WGK Germany ]

3
[HS Code ]

2914390090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Spectrum DetailBack Directory
[Spectrum Detail]

4-METHOXY-3-HYDROXYACETOPHENONE(6100-74-9)MS
4-METHOXY-3-HYDROXYACETOPHENONE(6100-74-9)1HNMR
4-METHOXY-3-HYDROXYACETOPHENONE(6100-74-9)IR1
4-METHOXY-3-HYDROXYACETOPHENONE(6100-74-9)IR2
6100-74-9 suppliers list
Company Name: Shanghai He-H Chemical Technology Co., Ltd  Gold
Telephone: 18621911604
Website: http://heh-chem.com/
Company Name: Sci-Sun Technology CO.,Ltd  Gold
Telephone: 18252089365
Website:
Company Name: J & K SCIENTIFIC LTD.  
Telephone: 18210857532 18210857532
Website: https://www.jkchemical.com
Company Name: Energy Chemical  
Telephone: 400-0056266
Website: www.energy-chemical.com
Company Name: Beijing Ouhe Technology Co., Ltd  
Telephone: 13552068683 13522913783
Website: www.ouhetech.cn/
Company Name: Jia Xing Isenchem Co.,Ltd  
Telephone: 0573-85285100 18627885956
Website: https://www.chemicalbook.com/ShowSupplierProductsList14265/0_EN.htm
Company Name: Accela ChemBio Co.,Ltd.  
Telephone: 021-50795510 4000665055
Website: http://www.shao-yuan.com/
Company Name: Shanghai Hanhong Scientific Co.,Ltd.  
Telephone: 021-54306202 13764082696
Website: https://www.hanhongsci.com
Company Name: Chemsky(shanghai)International Co.,Ltd.  
Telephone: 021-50135380
Website: www.shchemsky.com
Company Name: BioBioPha Co., Ltd.  
Telephone: 0871-65217109
Website: http://www.biobiopha.com
Company Name: Nanjing JinruiJiuAn Biotechnology Co., Ltd.  
Telephone: 025-58196018 800028039
Website: www.chemicalbook.com/ShowSupplierProductsList15703/0_EN.htm
Company Name: TargetMol Chemicals Inc.  
Telephone: 021-021-33632979 15002134094
Website: https://www.targetmol.cn/
Company Name: Shanghai Huikai Chemical Technology Co., Ltd.  
Telephone: 021-61995394 18916691159
Website: www.chemicalsea.com
Company Name: Bide Pharmatech Ltd.  
Telephone: 400-164-7117 18317119277
Website: www.bidepharm.com
Company Name: Quality Control Solutions Ltd.  
Telephone: 0755-66853366 13670046396
Website: www.qcsrm.com
Company Name: Wuxi Zhongkun Biochemical Technology Co., Ltd.  
Telephone: 0510-85629785 18013409632;
Website: www.reading-chemicals.com
Company Name: Shanghai Kewel Chemical Co., Ltd.  
Telephone: 021-64609169 18901607656
Website: http://www.kewelchem.com/
Company Name: Hangzhou J&H Chemical Co., Ltd.  
Telephone: 0571-87396432
Website: www.jhechem.com
Tags:6100-74-9 Related Product Information
855-96-9 3162-29-6 28281-49-4 2107-69-9 705-15-7 2879-20-1 4101-30-8 13909-73-4 1136-86-3 1131-62-0 552-41-0 498-02-2 4136-21-4 5396-18-9