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Chemical structure of CAS 66-99-9

2-Naphthaldehyde

In Stock•Starting at $7 for 1 g•Purity ≥ 98%
CAS No.66-99-9
MDL No.MFCD00004094
MFC11H8O
MW156.18
InChI KeyPJKVFARRVXDXAD-UHFFFAOYSA-N
CUSTOM SYNTHESISPRECLINICAL SUPPORT

Pricing & Availability

Pack SizePurityPriceAvailabilityAction
1 g98%$7In Stock
5 g98%$7In Stock
10 g98%$8In Stock
25 g98%$14In Stock
4*25 g98%$55In Stock
Custom synthesis and bulk supply options are available upon request.

Product Information

2-Naphthaldehyde is a naphthalene derivative substituted with a formyl group at the 2-position and functions as a mouse metabolite.

CAS No.66-99-9
Product Name2-Naphthaldehyde
IrritantIrritant
Signal Word:Warning
HCode:H302-H312-H315-H319-H332-H335
PCode:P261-P264-P264+P265-P270-P271-P280-P301+P317-P302+P352-P304+P340-P305+P351+P338-P317-P319-P321-P330-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501

Related Articles

Studies related to this compound and its mechanism of action

Inhibitory effects of cancer cell proliferation by novel histone deacetylase inhibitors involve p21/WAF1 induction and G2/M arrest.

Biological & pharmaceutical bulletin • Vol. 28, Issue 5 • 2005
PMID: 15863892DOI: 10.1248/bpb.28.849

Thermal growth and decomposition of methylnaphthalenes.

Environmental science & technology • Vol. 39, Issue 9 • 2005
PMID: 15926555DOI: 10.1021/es048537q

Evaluation of alpha-cyano ethers as fluorescent substrates for assay of cytochrome P450 enzyme activity.

Analytical biochemistry • Vol. 344, Issue 2 • 2005
PMID: 16083846PMC: PMC1450254DOI: 10.1016/j.ab.2005.06.032

Potent histone deacetylase inhibitors: N-hydroxybenzamides with antitumor activities.

Bioorganic & medicinal chemistry • Vol. 12, Issue 16 • 2004
PMID: 15265487DOI: 10.1016/j.bmc.2004.06.020

Documentation

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