2,3-Naphthalenediol structure
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Common Name | 2,3-Naphthalenediol | ||
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CAS Number | 92-44-4 | Molecular Weight | 160.17 | |
Density | 1.3±0.1 g/cm3 | Boiling Point | 353.9±15.0 °C at 760 mmHg | |
Molecular Formula | C10H8O2 | Melting Point | 161-165 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 181.0±15.0 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of 2,3-NaphthalenediolNaphthalene-2,3-diol is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
Name | naphthalene-2,3-diol |
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Synonym | More Synonyms |
Description | Naphthalene-2,3-diol is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
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Related Catalog | |
In Vitro | 2,3-二羟基萘用于制造染料、颜料、荧光增白剂、鞣剂、抗氧化剂和防腐剂。 |
Density | 1.3±0.1 g/cm3 |
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Boiling Point | 353.9±15.0 °C at 760 mmHg |
Melting Point | 161-165 °C(lit.) |
Molecular Formula | C10H8O2 |
Molecular Weight | 160.17 |
Flash Point | 181.0±15.0 °C |
Exact Mass | 160.052429 |
PSA | 40.46000 |
LogP | 2.11 |
Vapour Pressure | 0.0±0.8 mmHg at 25°C |
Index of Refraction | 1.726 |
Storage condition | 2-8°C |
Water Solubility | slightly soluble |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xi:Irritant |
Risk Phrases | R36/37/38 |
Safety Phrases | S26-S37/39 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
RTECS | QJ4750000 |
HS Code | 2907299090 |
Precursor 10 | |
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DownStream 10 | |
HS Code | 2907299090 |
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Summary | 2907299090 polyphenols; phenol-alcohols。supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward)。VAT:17.0%。tax rebate rate:9.0%。MFN tariff:5.5%。general tariff:30.0% |
Phase II metabolism in human skin: skin explants show full coverage for glucuronidation, sulfation, N-acetylation, catechol methylation, and glutathione conjugation.
Drug Metab. Dispos. 43(1) , 126-39, (2014) Although skin is the largest organ of the human body, cutaneous drug metabolism is often overlooked, and existing experimental models are insufficiently validated. This proof-of-concept study investig... |
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The syntheses and characterizations of molybdenum(VI) complexes with catechol and 2,3-dihydroxynaphthalene, and the structure-effect relationship in their in vitro anticancer activities.
Dalton Trans. 41(28) , 8697-702, (2012) The reactions of (NH(4))(2)Mo(2)O(7)·2H(2)O with polyhydroxy phenols (catechol or 2,3-dihydroxynaphthalene) and ethylenediamine (en), trimethylenediamine (tn), 1,2-propanediamine (pn), triethylamine (... |
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Selective antiproliferative activity of hydroxynaphthyl-beta-D-xylosides.
J. Med. Chem. 49 , 1932-8, (2006) The antiproliferative activity of the 14 isomeric monoxylosylated dihydroxynaphthalenes has been tested in vitro toward normal HFL-1 and 3T3 A31 cells as well as transformed T24 and 3T3 SV40 cells. Th... |
2,3-Dihydroxy naphthalene |
2,3-DIHYDROXY-NAPHTHALENE |
naphthalene-2,3-diol |
2,3-Naphthalenediol |
MFCD00004073 |
EINECS 202-156-7 |
2,3-dihydroxynaphthalene |