Home Bromides 629-04-9
629-04-9,MFCD00000273
Catalog No.:AA0032NE

629-04-9 | 1-Bromoheptane

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10g
95%
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$6.00   $4.00
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500g
>98.0%(GC)
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$102.00   $72.00
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  • Technical Information
  • Properties
  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA0032NE
Chemical Name:
1-Bromoheptane
CAS Number:
629-04-9
Molecular Formula:
C7H15Br
Molecular Weight:
179.0980
MDL Number:
MFCD00000273
SMILES:
CCCCCCCBr
NSC Number:
7315
Properties
Properties
 
BP:
180°C at 760 mmHg  
Form:
Liquid  
MP:
-58 °C(lit.)  
Refractive Index:
n20/D 1.4499(lit.)  
Solubility:
0.0066g/l  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
35.4  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
8  
Rotatable Bond Count:
5  
Undefined Atom Stereocenter Count:
1  
XLogP3:
4.4  

Literature

Title: Microwave-assisted preparation of the quorum-sensing molecule 2-heptyl-3-hydroxy-4(1H)-quinolone and structurally related analogs.

Journal: Nature protocols 20120524

Title: Preclinical genotoxicology of nor-β-lapachone in human cultured lymphocytes and Chinese hamster lung fibroblasts.

Journal: Chemical research in toxicology 20110919

Title: 3,3'-[1,2-Phenyl-enebis(methyl-ene)]bis-(1-heptyl-benzimidazolium) dibromide monohydrate.

Journal: Acta crystallographica. Section E, Structure reports online 20110701

Title: Synthesis and evaluation of quinonoid compounds against tumor cell lines.

Journal: European journal of medicinal chemistry 20110101

Title: Synthesis of truncated analogues of the iNKT cell agonist, α-galactosyl ceramide (KRN7000), and their biological evaluation.

Journal: Bioorganic & medicinal chemistry 20110101

Title: Ontogeny and season constrain the production of herbivore-inducible plant volatiles in the field.

Journal: Journal of chemical ecology 20101201

Title: Biochemical mechanism of caffeic acid phenylethyl ester (CAPE) selective toxicity towards melanoma cell lines.

Journal: Chemico-biological interactions 20101006

Title: 1,4-Di-n-hept-yloxy-2,5-dinitro-benzene.

Journal: Acta crystallographica. Section E, Structure reports online 20100101

Title: Biochemical mechanism of acetaminophen (APAP) induced toxicity in melanoma cell lines.

Journal: Journal of pharmaceutical sciences 20090401

Title: Biochemical mechanism of acetylsalicylic acid (Aspirin) selective toxicity toward melanoma cell lines.

Journal: Melanoma research 20081201

Title: Metabolic bioactivation and toxicity of ethyl 4-hydroxybenzoate in human SK-MEL-28 melanoma cells.

Journal: Journal of pharmaceutical sciences 20080501

Title: Biochemical basis of 4-hydroxyanisole induced cell toxicity towards B16-F0 melanoma cells.

Journal: Cancer letters 20061118

Title: The biosynthesis of ascorbate protects isolated rat hepatocytes from cumene hydroperoxide-mediated oxidative stress.

Journal: Free radical biology & medicine 20050401

Title: Glycogenolysis is directed towards ascorbate synthesis by glutathione conjugation.

Journal: Biochemical and biophysical research communications 20040423

Title: Glutathione depletion exacerbates methylenedianiline toxicity to biliary epithelial cells and hepatocytes in rats.

Journal: Toxicological sciences : an official journal of the Society of Toxicology 20030801

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