Detail of "2425-95-8"

MSDS Download
CAS Number:
2425-95-8
Name:
Benzenamine,4,4'-(1,3,4-oxadiazole-2,5-diyl)bis-
Superlist Name:
2,5-Bis(4-aminophenyl)-1,3,4-oxadiazole
Molecular Structure:
Formula:
C14H12 N4 O
Molecular Weight:
252.27
Synonyms:
1,3,4-Oxadiazole,2,5-bis(p-aminophenyl)- (6CI,7CI,8CI); 2,5-Bis(4-aminophenyl)-1,3,4-oxadiazole;2,5-Bis(4'-aminophenyl)-1,3,4-oxadiazole;2,5-Bis(p-aminophenyl)-1,3,4-oxadiazole; 2,5-Di(p-aminophenyl)-1,3,4-oxadiazole
Density:
1.301g/cm³
Melting Point:
250-254 °C(lit.)
Boiling Point:
508.1°Cat760mmHg
Flash Point:
261.1°C
Hazard Symbols:
Risk Codes:
36/37/38
Safety:
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37/39
WGK Germany 3

F 8-9-23
Details

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

Amine-cured epoxy/glass fiber composites: Amine-cured epoxy/glass fiber composites. Varma, Indra K.; Kothari, Madan L. (Cent. Mater. Sci. 65595-88-2 and 2425-95-8 are cas registry numbers. These chemicals are also mentioned in this article. Technol., Indian Inst. Technol., New Delhi 110 016, India). Indian J. Technol., 21(7), 265-7 (English) 1983. CODEN: IJOTA8. ISSN: 0019-5669. DOCUMENT TYPE: Journal CA Section: 37 (Plastics Manufacture and Processing) A series of composites were prepd. from epoxy resins cured with arom. amines of different mol. wt. and glass fabrics. The processing properties of the composites were similar to those of a control sample cured with 4,4'-diaminodiphenyl sulfone. Flexural strength and char yields of 3 of the arom. amine-cured epoxy-glass fabric composites were higher than those of the control samples. .

Organic photoconductor: Organic photoconductor. (Canon K. K., Japan). Jpn. Kokai Tokkyo Koho JP 58147746 A2 2 Sep 1983 Showa, 9 pp. (Japanese). (Japan). CODEN: JKXXAF. CLASS: IC: G03G005-06. APPLICATION: JP 82-31233 26 Feb 1982. DOCUMENT TYPE: Patent CA Section: 74 (Radiation Chemistry, Photochemistry, and Photographic and Other Reprographic Processes) A photoconductor for electrophotog. has the structure I (Z and Z1 = substituted or unsubstituted arylene; A and B = substituted or unsubstituted arom. hydrocarbon or heterocyclic ring; R, R1, R2, R3 = alkyl, aryl, aralkyl, or heterocyclic group). It has high photosensitivity and stable electrostatic characteristics during repeated charging and discharging processes. Thus, an electrophotog. plate was prepd. by coating an Al plate successively with an underlayer of casein, a charge-generating layer contg. compd. II with 0.5 mm thickness, and a charge-transfer layer contg. 87962-82-1 and 2425-95-8 are just another two chemicals used in this study. III with 12 mm thickness. The plate showed high light sensitivity and good electrostatic properties and was stable during 500 charging and discharging cycles. .