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38226-10-7,MFCD01090996
Catalog No.:AA003H83

38226-10-7 | 2-Fluoro-6-hydroxybenzaldehyde

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
97%
in stock  
$13.00   $9.00
- +
5g
97%
in stock  
$56.00   $39.00
- +
10g
97%
in stock  
$102.00   $72.00
- +
25g
98%
in stock  
$232.00   $163.00
- +
100g
98%
in stock  
$837.00 $586.00
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA003H83
Chemical Name:
2-Fluoro-6-hydroxybenzaldehyde
CAS Number:
38226-10-7
Molecular Formula:
C7H5FO2
Molecular Weight:
140.1118
MDL Number:
MFCD01090996
SMILES:
O=Cc1c(O)cccc1F
Properties
Properties
 
BP:
201.3°C at 760 mmHg  
Form:
Solid  
MP:
37-39°C  
Stability:
Air Sensitive  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
127  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0  
Rotatable Bond Count:
1  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
1.7  

Upstream Synthesis Route

[1]JournaloftheChemicalSociety-PerkinTransactions1,1997,#19,p.2925-2929

[2]Patent:US2017/37038,2017,A1,.Locationinpatent:Paragraph0096;0378;0382;0383

[1]JournaloftheChemicalSociety,PerkinTransactions1:OrganicandBio-OrganicChemistry(1972-1999),1994,#13,p.1823-1832

[2]EuropeanJournalofOrganicChemistry,2016,vol.2016,#7,p.1429-1438

[3]Patent:CN104557654,2017,B,.Locationinpatent:Paragraph0086-0088

[1]Patent:US2004/106653,2004,A1,.Locationinpatent:Page/Pagecolumn42

[2]Patent:WO2004/45610,2004,A1,.Locationinpatent:Page/Pagecolumn137-138

[1]JournalofOrganicChemistry,2006,vol.71,#9,p.3646-3649

[1]OrganicLetters,2017,vol.19,#23,p.6280-6283

Downstream Synthesis Route

[1]JournaloftheChemicalSociety.PerkintransactionsI,1994,p.1823-1832

[2]EuropeanJournalofOrganicChemistry,2016,vol.2016,p.1429-1438

[3]Patent:CN104557654,2017,B.Locationinpatent:Paragraph0086-0088

[1]ZeitschriftfurNaturforschung.TeilB.AnorganischeChemie,organischeChemie,Biochemie,Biophysik,Biologie,1972,vol.27,p.663-674

[1]ZeitschriftfurNaturforschung.TeilB.AnorganischeChemie,organischeChemie,Biochemie,Biophysik,Biologie,1972,vol.27,p.663-674

[1]ZeitschriftfurNaturforschung.TeilB.AnorganischeChemie,organischeChemie,Biochemie,Biophysik,Biologie,1972,vol.27,p.663-674

[1]JournalofOrganicChemistry,2006,vol.71,p.3646-3649

Literature
Quotation Request
Company Name:
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Additional Info:
Submit
SDS
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Tags:38226-10-7 Molecular Formula|38226-10-7 MDL|38226-10-7 SMILES|38226-10-7 2-Fluoro-6-hydroxybenzaldehyde
Catalog No.: AA003H83
38226-10-7,MFCD01090996
38226-10-7 | 2-Fluoro-6-hydroxybenzaldehyde
Pack Size： 1g
Purity： 97%
in stock
$13.00 $9.00
Pack Size： 5g
Purity： 97%
in stock
$56.00 $39.00
Pack Size： 10g
Purity： 97%
in stock
$102.00 $72.00
Pack Size： 25g
Purity： 98%
in stock
$232.00 $163.00
Pack Size： 100g
Purity： 98%
in stock
$837.00 $586.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA003H83
Chemical Name: 2-Fluoro-6-hydroxybenzaldehyde
CAS Number: 38226-10-7
Molecular Formula: C7H5FO2
Molecular Weight: 140.1118
MDL Number: MFCD01090996
SMILES: O=Cc1c(O)cccc1F
Properties
BP: 201.3°C at 760 mmHg  
Form: Solid  
MP: 37-39°C  
Stability: Air Sensitive  
Storage: Inert atmosphere;2-8℃;  
Complexity: 127  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Isotope Atom Count: 0  
Rotatable Bond Count: 1  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 1.7  
Upstream Synthesis Route
199388-02-8    38226-10-7 

[1]JournaloftheChemicalSociety-PerkinTransactions1,1997,#19,p.2925-2929

[2]Patent:US2017/37038,2017,A1,.Locationinpatent:Paragraph0096;0378;0382;0383

50-00-0    372-20-3    38226-10-7    348-28-7 

[1]JournaloftheChemicalSociety,PerkinTransactions1:OrganicandBio-OrganicChemistry(1972-1999),1994,#13,p.1823-1832

[2]EuropeanJournalofOrganicChemistry,2016,vol.2016,#7,p.1429-1438

[3]Patent:CN104557654,2017,B,.Locationinpatent:Paragraph0086-0088

146137-74-8    38226-10-7 

[1]Patent:US2004/106653,2004,A1,.Locationinpatent:Page/Pagecolumn42

[2]Patent:WO2004/45610,2004,A1,.Locationinpatent:Page/Pagecolumn137-138

888958-32-5    38226-10-7 

[1]JournalofOrganicChemistry,2006,vol.71,#9,p.3646-3649

446-52-6    38226-10-7 

[1]OrganicLetters,2017,vol.19,#23,p.6280-6283

Downstream Synthesis Route
50-00-0    372-20-3    38226-10-7    348-28-7 

[1]JournaloftheChemicalSociety.PerkintransactionsI,1994,p.1823-1832

[2]EuropeanJournalofOrganicChemistry,2016,vol.2016,p.1429-1438

[3]Patent:CN104557654,2017,B.Locationinpatent:Paragraph0086-0088

38226-10-7    38225-97-7 

[1]ZeitschriftfurNaturforschung.TeilB.AnorganischeChemie,organischeChemie,Biochemie,Biophysik,Biologie,1972,vol.27,p.663-674

38226-10-7    38226-04-9 

[1]ZeitschriftfurNaturforschung.TeilB.AnorganischeChemie,organischeChemie,Biochemie,Biophysik,Biologie,1972,vol.27,p.663-674

38226-09-4    38226-10-7 

[1]ZeitschriftfurNaturforschung.TeilB.AnorganischeChemie,organischeChemie,Biochemie,Biophysik,Biologie,1972,vol.27,p.663-674

888958-32-5    38226-10-7 

[1]JournalofOrganicChemistry,2006,vol.71,p.3646-3649

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