Home Other Building Blocks 3-Bromo-1-propanol

3-Bromo-1-propanol

CAS No.:
627-18-9
Catalog Number:
AG0035RD
Molecular Formula:
C3H7BrO
Molecular Weight:
138.9911
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
95%
In Stock USA
United States
$8
- +
25g
95%
In Stock USA
United States
$19
- +
100g
95%
In Stock USA
United States
$63
- +
500g
95%
In Stock USA
United States
$188
- +
Product Description
Catalog Number:
AG0035RD
Chemical Name:
3-Bromo-1-propanol
CAS Number:
627-18-9
Molecular Formula:
C3H7BrO
Molecular Weight:
138.9911
MDL Number:
MFCD00002942
IUPAC Name:
3-bromopropan-1-ol
InChI:
InChI=1S/C3H7BrO/c4-2-1-3-5/h5H,1-3H2
InChI Key:
RQFUZUMFPRMVDX-UHFFFAOYSA-N
SMILES:
OCCCBr
EC Number:
210-986-6
UNII:
3T4AXH68FH
Properties
Complexity:
16.4  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
137.968g/mol
Formal Charge:
0
Heavy Atom Count:
5  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
138.992g/mol
Monoisotopic Mass:
137.968g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
20.2A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.7  
Literature
Title Journal
Bis(μ(2)-4,7-dimethyl-4,7-diazadecane-1,10-dithiolato)trinickel(II) bis(perchlorate). Acta crystallographica. Section E, Structure reports online 20120301
3-(9H-Carbazol-9-yl)propan-1-ol. Acta crystallographica. Section E, Structure reports online 20110101
Synthesis and evaluation of amino acid-based radiotracer 99mTc-N4-AMT for breast cancer imaging. Journal of biomedicine & biotechnology 20110101
Glycoconjugates, products of uridine derivatives phosphitylation and oxidation as glycosyltransferases potential inhibitors. Acta poloniae pharmaceutica 20100101
Analysis of vibrational spectra of 3-halo-1-propanols CH(2)XCH(2)CH(2)OH (X is Cl and Br). Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20081201
Halogenated derivatives QSAR model using spectral moments to predict haloacetic acids (HAA) mutagenicity. Bioorganic & medicinal chemistry 20080515
Development of indole chemistry to label tryptophan residues in protein for determination of tryptophan surface accessibility. Protein science : a publication of the Protein Society 20070601
Synthesis of mono- and disaccharide analogs of moenomycin and lipid II for inhibition of transglycosylase activity of penicillin-binding protein 1b. Bioorganic & medicinal chemistry 20041215
Use of self-assembled surfactant systems as media for a substitution reaction. Journal of colloid and interface science 20040901
Steady-state and pre-steady-state kinetic analysis of halopropane conversion by a rhodococcus haloalkane dehalogenase. Biochemistry 20030708
Chloride-sensitive fluorescent indicators. Analytical biochemistry 20010601
Properties