Detail of "695-99-8"

CAS Number:
695-99-8
Name:
2,5-Cyclohexadiene-1,4-dione,2-chloro-
Molecular Structure:
Formula:
C₆H₃ClO₂
Molecular Weight:
142.54
Synonyms:
p-Benzoquinone,2-chloro- (8CI);p-Benzoquinone, chloro- (6CI,7CI);2-Chloro-1,4-benzoquinone;2-Chloro-2,5-cyclohexadiene-1,4-dione;2-Chloro-p-benzoquinone;2-Chloroquinone;Chloro-1,4-benzoquinone;Chloro-p-benzoquinone;Chloroquinone;Monochloro-p-benzoquinone;Monochloroquinone;NSC 526777;
Density:
1.4 g/cm³
Melting Point:
52-57 °C
Boiling Point:
210.1 °C at 760 mmHg
Flash Point:
83.2 °C
Appearance:
yellow to brown crystals
Hazard Symbols:
Xi
Risk Codes:
36/37/38
Safety:
26-37/39 Details

Supplier Location
Supplier Location
- China (Mainland)(2)
Business Type
Business Type
- Lab/Research institutions(1)
- Manufacturers(0)
- Trading Company(1)
Certificates
Certificates
- ISO (0)
- Production License (0)

Display：

Supplier:Hangzhou Share Chemical Co., Ltd [ China (Mainland)]

Verified-Platinum Supplier 1st Year Platinum
Supplier 920 Integral
920

Tel:+86-57187093700

Address:Hang Xing Road

C6H3ClO2

620 Integral
620

Tel:+86-010-81897556/60300056

Address:No 58 LiangGuan Rd, LiangXiang Development Zone, Fangshan District, BeiJing 102488, P.R. China

Please post your buying leads,so that our qualified suppliers will soon contact you!
*Required Fields

New components for charge-transfer complexes: New components for charge-transfer complexes. I. 2,5-Dibromo-3,6-dicyano-p-benzoquinone. Kampars, V.; Neilands, O. (Rizh. Politekh. Inst., Riga, USSR). Zh. Obshch. 393-40-8 and 695-99-8 which are cas registry numbers are also used here. Khim., 47(1), 150-3 (Russian) 1977. CODEN: ZOKHA4. DOCUMENT TYPE: Journal CA Section: 22 (Physical Organic Chemistry) The ionization potentials of a series of strong acceptors, esp. p-benzoquinones, were detd. spectrophotometrically in relation to their charge-transfer complexing behavior with donors such as anthracene, naphthalene, and pyrene; I was an esp. strong acceptor, with an electron affinity of 3.0 eV. The electron affinity of monosubstituted (Cl, Br, cyano) p-benzoquinones depended but little on mutual substituent orientations, and was well described by empirical substituent increments. .