ChemicalBook >> CAS DataBase List >>1,2-DIBENZOYLETHANE

1,2-DIBENZOYLETHANE

CAS No.
495-71-6
Chemical Name:
1,2-DIBENZOYLETHANE
Synonyms
Biphenacyl;NSC 402168;DIBENZOYL ETHANE;1,2-DIBENZOYLETHANE;TIMTEC-BB SBB008126;2,2''-Biacetophenone;2,2’’-biacetophenone;Ethane, 1,2-dibenzoyl-;β-Benzoylpropiophenone;1 2-DIBENZOYLETHANE 95%
CBNumber:
CB7233274
Molecular Formula:
C16H14O2
Molecular Weight:
238.28
MDL Number:
MFCD00037818
MOL File:
495-71-6.mol
MSDS File:
SDS
Last updated:2023-06-08 17:06:35

1,2-DIBENZOYLETHANE Properties

Melting point 144-145°C
Boiling point 260 °C / 15mmHg
Density 1.116±0.06 g/cm3(Predicted)
storage temp. Refrigerator
solubility Dichloromethane (Slightly), DMSO (Slightly), Chloroform (Slightly), Methanol (Slightly)
form Solid
color White to Off-White
Water Solubility Soluble in acetone. Insoluble in water.
BRN 782937
CAS DataBase Reference 495-71-6(CAS DataBase Reference)
NIST Chemistry Reference 1,4-Butanedione, 1,4-diphenyl-(495-71-6)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338
Safety Statements  22-24/25
HS Code  2914.39.9000
NFPA 704
1
0 0

1,2-DIBENZOYLETHANE price More Price(21)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical D3179 1,4-Diphenyl-1,4-butanedione >98.0%(GC) 495-71-6 1g $54 2024-03-01 Buy
Alfa Aesar L08652 1,2-Dibenzoylethane, 98+% 495-71-6 1g $57.65 2024-03-01 Buy
Alfa Aesar L08652 1,2-Dibenzoylethane, 98+% 495-71-6 5g $212 2024-03-01 Buy
Usbiological 008983 1,2-Dibenzoylethane 495-71-6 1g $403 2021-12-16 Buy
TRC D417320 1,2-Dibenzoylethane 495-71-6 10g $875 2021-12-16 Buy
Product number Packaging Price Buy
D3179 1g $54 Buy
L08652 1g $57.65 Buy
L08652 5g $212 Buy
008983 1g $403 Buy
D417320 10g $875 Buy

1,2-DIBENZOYLETHANE Chemical Properties,Uses,Production

Uses

1,2-Dibenzoylethane is effective in inhibiting the in vivo mammary DMBA-DNA adduct formation. This inhibitory effect on mammary DNA adduct formation was associated with increased liver activities of glutathione S-transferase, QR, and 7-ethoxyresorufin-O-deethylase.

Uses

It is effective in inhibiting the in vivo mammary DMBA-DNA adduct formation. This inhibitory effect on mammary DNA adduct formation was associated with increased liver activities of glutathione S-transferase, QR, and 7-ethoxyresorufin-O-deethylase.

Synthesis Reference(s)

Chemical and Pharmaceutical Bulletin, 28, p. 262, 1980 DOI: 10.1248/cpb.28.262
Journal of the American Chemical Society, 91, p. 687, 1969 DOI: 10.1021/ja01031a029
Tetrahedron Letters, 29, p. 3717, 1988 DOI: 10.1016/S0040-4039(00)82162-0

1,2-DIBENZOYLETHANE Preparation Products And Raw materials

Raw materials

Preparation Products

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1,4-diphenyl-1,4-butadione 2,2’’-biacetophenone 2,2''-Biacetophenone Biphenacyl Ethane, 1,2-dibenzoyl- TIMTEC-BB SBB008126 DIBENZOYL ETHANE 1,4-DIPHENYL-BUTANE-1,4-DIONE 1,4-DIPHENYL-1,4-BUTANEDIONE 1,2-DIBENZOYLETHANE 1,2-DIBENZOYLETHANE 98+% 1 2-DIBENZOYLETHANE 95% β-Benzoylpropiophenone 1,4-Dioxo-1,4-diphenylbutane NSC 402168 1 4-DIPHENYL-1 4-BUTANEDIONE 95% 1,4-Diphenyl-1,4-butanedione> 1,4-Butanedione, 1,4-diphenyl- 1,2-DIBENZOYLETHANE ISO 9001:2015 REACH 495-71-6 C6H5COCH2CH2COC6H5 Aromatics Inhibitors Intermediates & Fine Chemicals Pharmaceuticals Miscellaneous