Results for:
chemical Classification: boron compounds

Butylboronic Acid

Compound Details

Synonymous names
n-Butylboronic acid
4426-47-5
1-butylboronic acid
BUTYLBORONIC ACID
1-Butaneboronic acid
1-BUTANE BORONIC ACID
Boronic acid, butyl-
Butyl boronic acid
n-Butaneboronic acid
MFCD00002106
butaneboronic acid
CHEMBL31962
1-Butyldihydroxyborane
N-butylboronate
1-butylboronicacid
BUB
4-butylboronic acid
EINECS 224-607-7
n-butyl boronic acid
n-butane boronic acid
Butylboronic acid, 97%
SCHEMBL15975
QPKFVRWIISEVCW-UHFFFAOYSA-
DTXSID90196087
BCP22759
STR06559
BDBM50067884
AKOS005254957
BCP9000049
CS-W000932
DB02664
NCGC00249446-01
SY012742
DB-010279
B0529
NS00073507
1-(Dihydroxyboryl)butane; n-Butylboronic acid
A19498
EN300-179386
W-106206
Q27093616
Butylboronic acid, for GC derivatization, >=96.0% (T)
F0001-1206
Z1147227739
InChI=1/C4H11BO2/c1-2-3-4-5(6)7/h6-7H,2-4H2,1H3
Microorganism:

Yes

IUPAC namebutylboronic acid
SMILESB(CCCC)(O)O
InchiInChI=1S/C4H11BO2/c1-2-3-4-5(6)7/h6-7H,2-4H2,1H3
FormulaC4H11BO2
PubChem ID20479
Molweight101.94
LogP0
Atoms7
Bonds3
H-bond Acceptor2
H-bond Donor2
Chemical Classificationacids boron compounds

mVOC Specific Details

Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaSaccharomyces CerevisiaeNANAHarris et al. 2021
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaSaccharomyces Cerevisiaemalt extract brothHS-SPME with GC-MSno


1-(9-borabicyclo[3.3.1]nonan-9-yl)-3,5-ditert-butylpyrazole

Compound Details

Synonymous names
SZXOLJDCCBPVMW-UHFFFAOYSA-N
1-(9-Borabicyclo[3.3.1]non-9-yl)-3,5-ditert-butyl-1H-pyrazole #
1H-Pyrazole, 1-(9-borabicyclo[3.3.1]non-9-yl)-3,5-bis(1,1-dimethylethyl)-
Microorganism:

Yes

IUPAC name1-(9-borabicyclo[3.3.1]nonan-9-yl)-3,5-ditert-butylpyrazole
SMILESB1(C2CCCC1CCC2)N3C(=CC(=N3)C(C)(C)C)C(C)(C)C
InchiInChI=1S/C19H33BN2/c1-18(2,3)16-13-17(19(4,5)6)22(21-16)20-14-9-7-10-15(20)12-8-11-14/h13-15H,7-12H2,1-6H3
FormulaC19H33BN2
PubChem ID618108
Molweight300.3
LogP0
Atoms22
Bonds3
H-bond Acceptor1
H-bond Donor0
Chemical Classificationaromatic compounds boron compounds heterocyclic compounds nitrogen compounds pyrazoles

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
Pectobacterium CarotovorumKate et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
Pectobacterium Carotovoruminoculated potato samplesGC-MSno


[(E)-3-[9-borabicyclo[3.3.1]nonan-9-yloxy(ethyl)boranyl]pent-2-en-2-yl]-trimethylgermane

Compound Details

Synonymous names
ADRXUIHYPYTXKG-SDXDJHTJSA-N
((1E)-2-[(9-Borabicyclo[3.3.1]non-9-yloxy)(ethyl)boryl]-1-methyl-1-butenyl)(trimethyl)germane #
9-Borabicyclo[3.3.1]nonane, 9-[[ethyl[1-ethyl-2-(trimethylgermyl)-1-propenyl]boryl]oxy]-, (Z)-
Microorganism:

No

IUPAC name[(E)-3-[9-borabicyclo[3.3.1]nonan-9-yloxy(ethyl)boranyl]pent-2-en-2-yl]-trimethylgermane
SMILESB1(C2CCCC1CCC2)OB(CC)C(=C(C)[Ge](C)(C)C)CC
InchiInChI=1S/C18H36B2GeO/c1-7-18(15(3)21(4,5)6)19(8-2)22-20-16-11-9-12-17(20)14-10-13-16/h16-17H,7-14H2,1-6H3/b18-15-
FormulaC18H36B2GeO
PubChem ID5370816
Molweight362.7
LogP0
Atoms22
Bonds6
H-bond Acceptor1
H-bond Donor0
Chemical Classificationboron compounds germanium compounds

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
Aspergillus FlavusKate et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
Aspergillus Flavusinoculated potato samplesGC-MSno