2-Bromohexadecanoic acid - CAS 18263-25-7

Name: 2-Bromohexadecanoic acid
Brand: BOC Sciences
Rating: 5 (1 reviews)

Catalog:	BB014011
Product Name:	2-Bromohexadecanoic acid
CAS:	18263-25-7
Synonyms:	2-bromohexadecanoic acid

Technical Data

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Computed Properties

IUPAC Name:	2-bromohexadecanoic acid
Description:	2-Bromohexadecanoic acid (CAS# 18263-25-7) is used in preparation of substituted purines and their analogs for inhibiting the expression of a pattern recognition receptor.
Molecular Weight:	335.32
Molecular Formula:	C16H31BrO2
Canonical SMILES:	CCCCCCCCCCCCCCC(C(=O)O)Br
InChI:	InChI=1S/C16H31BrO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15(17)16(18)19/h15H,2-14H2,1H3,(H,18,19)
InChI Key:	DPRAYRYQQAXQPE-UHFFFAOYSA-N
Boiling Point:	403.4 °C at 760 mmHg
Purity:	98 %
Density:	1.114 g/cm³
Appearance:	White crystalline powder
MDL:	MFCD00004215
LogP:	5.92570

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Related Functional Groups

Carbonyl Compounds

[5650-34-0]C9H8O2
Oxiran-2-yl(phenyl)methanone
[51493-02-8]C5H10ClNO
N-Methyl-N-propylcarbamoyl Chloride
[1427004-19-0]C34H39N3O10
DBCO-PEG4-NHS ester
[1383427-98-2]C7H13ClN2O2
(S)-Hexahydropyrazino[2,1-c][1,4]oxazin-4(3H)-one hydrochloride
[70199-62-1]C8H10ClNO
(4-Pyridyl)acetone Hydrochloride
[956439-56-8]C6H5N3O6
1-(Carboxymethyl)-3-nitro-1H-pyrazole-5-carboxylic acid

GHS Hazard Statement:	H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
Precautionary Statement:	P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501
Signal Word:	Warning

Publication Number	Title	Priority Date
CN-113215162-A	Reduction of Al-induced Abeta1-42Expression level interfering RNA and application thereof	20210602
CN-112479971-A	2-bromo-1- (7-nitroindoline) hexadecanone compound and preparation method and application thereof	20201209
CN-111789833-A	Application of 2-bromopalmitic acid in preparation of medicine for preventing and treating bone loss related diseases	20200831
KR-102174457-B1	Compounds for quantum dot ligand comprising a (meth)acrylate structure having carboxyl group, quantum dot particles comprising quantum dot ligands formed by the compounds, and composition comprising the quantum dot particles, and preparation method of the compounds	20200603
KR-102207330-B1	Compounds for quantum dot ligand comprising a (meth)acrylate structure having carboxyl group, quantum dot particles comprising quantum dot ligands formed by the compounds, and composition comprising the quantum dot particles, and preparation method of the compounds	20200603

PMID	Publication Date	Title	Journal
30076181	20190101	2-Bromopalmitate targets retinoic acid receptor alpha and overcomes all-trans retinoic acid resistance of acute promyelocytic leukemia	Haematologica
23001822	20121201	Linker for activation of T-cell family member2 (LAT2) a lipid raft adaptor protein for AKT signaling, is an early mediator of alkylphospholipid anti-leukemic activity	Molecular & cellular proteomics : MCP
22753418	20120817	Amino-terminal cysteine residues differentially influence RGS4 protein plasma membrane targeting, intracellular trafficking, and function	The Journal of biological chemistry
22562470	20120801	Plasma membrane localization is required for RasA-mediated polarized morphogenesis and virulence of Aspergillus fumigatus	Eukaryotic cell
22728137	20120730	RING finger palmitoylation of the endoplasmic reticulum Gp78 E3 ubiquitin ligase	FEBS letters

Complexity:	207
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	334.15074
Formal Charge:	0
Heavy Atom Count:	19
Hydrogen Bond Acceptor Count:	2
Hydrogen Bond Donor Count:	1
Isotope Atom Count:	0
Monoisotopic Mass:	334.15074
Rotatable Bond Count:	14
Topological Polar Surface Area:	37.3 Å²
Undefined Atom Stereocenter Count:	1
Undefined Bond Stereocenter Count:	0
XLogP3:	7.8