Methanone,(6-hydroxy-2-naphthalenyl)phenyl-

Names

[ Name ]:
Methanone,(6-hydroxy-2-naphthalenyl)phenyl-

[Synonym ]:
6-hydroxy-2-benzoylnaphthalene
6-Benzoyl-2-naphthol
Naphthalene,2-hydroxy-6-benzoyl
EINECS 257-755-6
MFCD00004107
6-Hydroxy-2-naphthyl phenyl ketone
Ketone,6-hydroxy-2-naphthyl phenyl

Chemical & Physical Properties

[ Density]:
1.24g/cm3

[ Boiling Point ]:
453.8ºC at 760mmHg

[ Melting Point ]:
161-162ºC(lit.)

[ Molecular Formula ]:
C₁₇H₁₂O₂

[ Molecular Weight ]:
248.27600

[ Flash Point ]:
193.3ºC

[ Exact Mass ]:
248.08400

[ PSA ]:
37.30000

[ LogP ]:
3.77640

[ Index of Refraction ]:
1.681

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :: OB4360000

CHEMICAL NAME :: Ketone, 6-hydroxy-2-naphthyl phenyl

CAS REGISTRY NUMBER :: 52222-87-4

BEILSTEIN REFERENCE NO. :: 3294044

LAST UPDATED :: 199612

DATA ITEMS CITED :: 1

MOLECULAR FORMULA :: C17-H12-O2

MOLECULAR WEIGHT :: 248.29

WISWESSER LINE NOTATION :: L66J CVR& HQ

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

MUTATION DATA

TYPE OF TEST :: Morphological transformation

TEST SYSTEM :: Rodent - hamster Kidney

DOSE/DURATION :: 80 ug/L

REFERENCE :: BJCAAI British Journal of Cancer. (Macmillan Press Ltd., Houndmills, Basingstoke, Hants. RG21 2XS, UK) V.1- 1947- Volume(issue)/page/year: 37,873,1978

Safety Information

[ Symbol ]:

GHS07

[ 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

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ RTECS ]:
OB4360000

[ HS Code ]:
2914501900

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2914501900

[ Summary ]:
2914501900 other ketone-phenols。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:5.5%。General tariff:30.0%

Articles

The histochemical demonstration of acid phosphatase by a post-incubation coupling technique.

J. Histochem. Cytochem. 3(6) , 455-70, (1955)

Histochemical demonstration of aryl sulfatase.

Science 116(3020) , 539-43, (1952)

Related Compounds

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