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86-52-2,MFCD00004042
Catalog No.:AA0032O5

86-52-2 | 1-Chloromethyl naphthalene

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1g
95%
in stock  
$24.00   $17.00
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5g
98%
in stock  
$29.00   $20.00
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25g
98%
in stock  
$45.00   $32.00
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100g
98%
in stock  
$112.00   $78.00
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500g
≥95.0%(GC)
in stock  
$411.00   $288.00
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  • Technical Information
  • Properties
  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA0032O5
Chemical Name:
1-Chloromethyl naphthalene
CAS Number:
86-52-2
Molecular Formula:
C11H9Cl
Molecular Weight:
176.6422
MDL Number:
MFCD00004042
SMILES:
ClCc1cccc2c1cccc2
NSC Number:
8473
Properties
Properties
 
BP:
167-169°C at 760 mmHg  
Form:
Liquid  
MP:
32 °C(lit.)  
Refractive Index:
n20/D 1.635(lit.)  
Stability:
Moisture Sensitive  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
144  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Rotatable Bond Count:
1  
XLogP3:
3.7  

Literature

Title: Palladium-catalyzed amination of chloromethylnaphthalene and chloromethylanthracene derivatives with various amines.

Journal: Journal of the American Chemical Society 20120328

Title: Synthesis and application of highly reactive amino linkers for functional oligonucleotides.

Journal: Current protocols in nucleic acid chemistry 20120301

Title: Molecular structure, polarizability, hyperpolarizability analysis and spectroscopic characterization of 1-(chloromethyl)-2-methylnaphthalene with experimental (FT-IR and FT-Raman) techniques and quantum chemical calculations.

Journal: Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20120101

Title: 3,14-Dimethyl-2,6,13,17-tetra-aza-tricyclo-[16.4.0.0]docosa-ne-(naphthalen-1-yl)methanol (1/2).

Journal: Acta crystallographica. Section E, Structure reports online 20120101

Title: Nucleophilic dearomatization of chloromethyl naphthalene derivatives via η3-benzylpalladium intermediates: a new strategy for catalytic dearomatization.

Journal: Organic letters 20111007

Title: Distributed Drug Discovery, Part 3: using D(3) methodology to synthesize analogs of an anti-melanoma compound.

Journal: Journal of combinatorial chemistry 20090112

Title: Distributed Drug Discovery, Part 2: global rehearsal of alkylating agents for the synthesis of resin-bound unnatural amino acids and virtual D(3) catalog construction.

Journal: Journal of combinatorial chemistry 20090112

Title: 1-(4-Methyl-1-naphth-yl)ethanone.

Journal: Acta crystallographica. Section E, Structure reports online 20081201

Title: Occupational contact dermatitis (drug-induced medicamentosa): six case reports.

Journal: International journal of immunopathology and pharmacology 20070101

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Tags:86-52-2 Molecular Formula|86-52-2 MDL|86-52-2 SMILES|86-52-2 1-Chloromethyl naphthalene |Organic_Building_Blocks