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Molecule
ID:10770
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₃H₁₅BBrNO₄
Molecular Mass
339.9775
Exact Mass
339.02775037
Charge
0
InChI
InChI=1S/C13H15BBrNO4/c1-13(2,3)20-12(17)16-10-5-4-9(15)6-8(10)7-11(16)14(18)19/h4-7,18-19H,1-3H3
InChIKey
RBYTXZMVOGZESQ-UHFFFAOYSA-N
Canonic Smiles
Brc1ccc2c(c1)cc(n2C(=O)OC(C)(C)C)B(O)O
Isomeric Smiles
n1(c(cc2cc(ccc12)Br)B(O)O)C(=O)OC(C)(C)C
Calculated Properties
JChem
Acid pKa
8.20348
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
3.459446
LogD (pH = 7.4)
3.3971977
Log P
3.4603
Molar Refractivity
73.2656
Polarizability
31.467379
Polar Surface Area
71.69
Rotatable Bonds
3
Lipinski's Rule of Five
true
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Registration numbers
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Properties
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Related Proteins
No Data Available
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Molecular Spectra
No Data Available
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Molecule Details
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References
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Bioactivity
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IUPAC Traditional name
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IUPAC name
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Synonyms
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MDL Number
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CAS Number
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PubChem CID
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PubChem SID
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Product Information
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Physical Property
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Molecular Spectra
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Sigma Aldrich
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR14252
Matrix Scientific
007672
Maybridge
MO01243
Sigma Aldrich
637394
Alfa Aesar
H32185
A&J Pharmtech
AJA-O32923
Academic Data
PubChem
2794714
Names and Identifiers
IUPAC Traditional name
5-bromo-1-(tert-butoxycarbonyl)indol-2-ylboronic acid
IUPAC name
{5-bromo-1-[(tert-butoxy)carbonyl]-1H-indol-2-yl}boronic acid
Synonyms
5-Bromo-N-(Boc)indole-2-boronic acid
5-Bromo-1H-indole-2-boronic acid, N-BOC protected
5-Bromo-1-(tert-butoxycarbonyl)-1H-indol-2-yl boronic acid
5-bromo-1-(tert-butoxycarbonyl)-1H-indol-2-ylboronic acid
1-(tert-Butoxycarbonyl-5-bromo-1H-indol-2-yl)boronic acid
N-(Boc-5-溴-2-吲哚基)硼酸
(N-Boc-5-bromo-2-indolyl)boronic acid
1-(叔丁氧羰基-5-溴-1H-吲哚-2-基)硼酸
5-Bromo-1-tert-butoxycarbonyl-1H-indole-2-boronic acid
1-Boc-5-溴吲哚-2-硼酸
1-Boc-5-bromoindole-2-boronic acid
Registration numbers
MDL Number
MFCD03701683
CAS Number
475102-13-7
PubChem CID
2794714
PubChem SID
160974077
24882851
Properties
Product Information
Purity
97%
Source
95%
Source
98%
Source
Empirical Formula (Hill Notation)
C13H15BBrNO4
Source
Safety Information
MSDS Link
Download link
Source
Download link
Source
TSCA Listed
false
Source
否
Source
Storage Warning
Irritant/Keep Cold
Source
German water hazard class
3
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
GHS Precautionary statements
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
Risk Statements
36/37/38
Source
European Hazard Symbols
Irritant (Xi)
Source
Safety Statements
26
-
37
Source
Physical Property
Melting Point
130 °C (dec.)(lit.)
Source
Molecule Details
Sigma Aldrich
637394
Packaging
1 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay