Benzo(c)phenanthrene structure
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Common Name | Benzo(c)phenanthrene | ||
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CAS Number | 195-19-7 | Molecular Weight | 228.288 | |
Density | 1.2±0.1 g/cm3 | Boiling Point | 436.7±12.0 °C at 760 mmHg | |
Molecular Formula | C18H12 | Melting Point | 158-160℃ | |
MSDS | Chinese USA | Flash Point | 209.1±13.7 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Name | Benzo[c]phenanthrene |
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Synonym | More Synonyms |
Density | 1.2±0.1 g/cm3 |
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Boiling Point | 436.7±12.0 °C at 760 mmHg |
Melting Point | 158-160℃ |
Molecular Formula | C18H12 |
Molecular Weight | 228.288 |
Flash Point | 209.1±13.7 °C |
Exact Mass | 228.093903 |
LogP | 5.91 |
Vapour Pressure | 0.0±0.5 mmHg at 25°C |
Index of Refraction | 1.771 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
MUTATION DATA
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Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H302 + H312 + H332-H315-H319-H335 |
Precautionary Statements | P261-P280-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xn: Harmful; |
Risk Phrases | 20/21/22-36/37/38 |
Safety Phrases | 26-37/39 |
RIDADR | UN 2811 |
RTECS | DI8225000 |
Packaging Group | III |
Hazard Class | 6.1(b) |
HS Code | 2902909090 |
HS Code | 2902909090 |
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Summary | 2902909090 other aromatic hydrocarbons。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:2.0%。General tariff:30.0% |
Benzo[c]phenanthrene adducts and nogalamycin inhibit DNA transesterification by vaccinia topoisomerase.
J. Biol. Chem. 279(22) , 23335-42, (2004) Vaccinia DNA topoisomerase forms a covalent DNA-(3'-phosphotyrosyl)-enzyme intermediate at a specific target site 5'-C(+5)C(+4)C(+3)T(+2)T(+1)p downward arrow N(-1) in duplex DNA. Here we study the ef... |
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In vitro and in vivo modulations of benzo[c]phenanthrene-DNA adducts by DNA mismatch repair system.
Nucleic Acids Res. 31(22) , 6428-34, (2003) Benzo[c]phenanthrene dihydrodiol epoxide (B[c] PhDE) is well known as an important environmental chemical carcinogen that preferentially modifies DNA in adenine residues. However, the molecular mechan... |
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Structure/reactivity relationships in the benzo[c]phenanthrene skeleton: stable ion and electrophilic substitution (nitration, bromination) study of substituted analogues, novel carbocations and substituted derivatives.
J. Org. Chem. 72(9) , 3232-41, (2007) A series of novel carbocations were generated by low-temperature protonation of substituted benzo[c]phenanthrenes, B[c]Phs, and their charge delocalization pathways were elucidated by NMR on the basis... |
Benzo[c]phenanthrene |
1S-TRANS-ANTI-BENZO[C]PHENANTHRENE |
AR-G 3 BENZO(C)PHENANTHRENE |
1R-TRANS-ANTI-BENZO[C]PHENANTHRENE |
Benzo(c)phenanthrene |
tetrahelicene |