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cis-1,2,3,6-????????????

cis-1,2,3,6-????????????
cis-1,2,3,6-???????????? ??? ???
?? ??:
935-79-5
???:
cis-1,2,3,6-????????????
???(??):
cis-1,2,3,6-????????????
???:
cis-1,2,3,6-Tetrahydrophthalic anhydride
???(??):
THPA;CIS-4-CYCLOHEXENE-1,2-DICARBOXYLIC ANHYDRIDE;4-CYCLOHEXENE-1,2-DICARBOXYLIC ANHYDRIDE;CIS-4-CYCLOHEXEN-1,2-DIMETHANOIC ANHYDRIDE;(3aR,7aS)-3a,4,7,7a-tetrahydroisobenzofuran-1,3-dione;CIS-THPA;cis-1,2,3,6-Tetrahyd;cis-1,2,3,6-TetrahydrophthaL;Cis-1,2,3,6-Tetrahydrophthalic;6-Tetrahydrophthalic anhydride
CBNumber:
CB5728570
???:
C8H8O3
??? ??:
152.15
MOL ??:
935-79-5.mol
MSDS ??:
SDS

cis-1,2,3,6-???????????? ??

???
98 °C
?? ?
234.6°C (rough estimate)
??
1.2143 (rough estimate)
?? ??
5.2 (vs air)
???
<0.01 mm Hg ( 20 °C)
???
1.4447 (estimate)
???
156 °C
?? ??
under inert gas (nitrogen or Argon) at 2-8°C
???
soluble in Toluene,Benzene
??? ??
powder to crystal
??
???? ?? ??
???
?? ??
??
Moisture Sensitive
BRN
82341
?? ??
ACGIH: TWA 0.01 mg/m3
OSHA: TWA 0.25 ppm(1 mg/m3)
NIOSH: IDLH 10 mg/m3; TWA 0.25 ppm(1 mg/m3)
CAS ??????
935-79-5(CAS DataBase Reference)
NIST
cis-1,2,3,6-Tetrahydrophthalic anhydride(935-79-5)
EPA
1,3-Isobenzofurandione, 3a,4,7,7a-tetrahydro-, (3aR,7aS)-rel- (935-79-5)
??
  • ?? ? ?? ??
  • ?? ? ???? ?? (GHS)
??? ?? Xn
?? ???? ?? 41-42/43-52/53
????? 22-24-26-37/39-61-52/53-42/43-41
????(UN No.) UN 2698 8/PG 3
WGK ?? 3
RTECS ?? GW5775000
TSCA Yes
?? ?? 8
???? III
HS ?? 29173990
????(GHS): GHS hazard pictogramsGHS hazard pictograms
?? ?: Danger
??·?? ??:
?? ??·?? ?? ?? ?? ?? ?? ? ?? ?? P- ??
H317 ????? ?? ??? ??? ? ?? ?? ??? ?? ?? 1 ?? GHS hazard pictograms P261, P272, P280, P302+P352,P333+P313, P321, P363, P501
H318 ?? ?? ??? ??? ?? ? ?? ?? ??? ?? ?? 1 ?? GHS hazard pictograms P280, P305+P351+P338, P310
H334 ?? ? ????? ??, ?? ?? ?? ?? ?? ??? ? ?? ??? ??? ?? ?? 1 ?? GHS hazard pictograms P261, P285, P304+P341, P342+P311,P501
H412 ??? ??? ?? ????? ??? ?? ????? ?? - ?? ?? 3 P273, P501
??????:
P261 ??·?·??·???·??·...·????? ??? ????.
P273 ???? ???? ???.
P280 ????/???/???/?????? ?????.
P302+P352 ??? ??? ??? ?? ????.
P305+P351+P338 ?? ??? ? ?? ?? ???? ????. ???? ?????? ?????. ?? ????.
NFPA 704
1
2 1

cis-1,2,3,6-???????????? MSDS


cis-4-Cyclohexene-1,2-dicarboxylic anhydride

cis-1,2,3,6-???????????? C??? ??, ??, ??

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Tetrahydrophthalic anhydride is an organic compound with the formula C6H8C2O3. The compound exists as two isomers, this article being focused on the more common cis isomer. It is a precursor to other compounds including the dicarboxylic acid tetrahydrophthalic acid as well the tetrahydrophthalimide, which is a precursor to the fungicide Captan. It is a white solid that is soluble in organic solvents.
Tetrahydrophthalic anhydride, the cis isomer, is prepared by the Diels-Alder reaction of butadiene and maleic anhydride.

??? ??

Tetrahydrophthalic Anhydride (THPA) is a white crystalline powder or FLAKES. It is slightly soluble in benzene and acetone and it is also sensitive to moisture.

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Tetrahydrophthalic Anhydride is an anhydride hardener mainly used in the fields of coatings, epoxy resin curing agents, polyester resins, adhesives, plasticizers, pesticides, etc. It is also used as a chemical intermediate for light colored alkyds.
Tetrahydrophthalic Anhydride is an organic compound obtained from the reaction of Maleic Anhydride and Butadiene.

?? ??

A flask containing 500 ml of dry benzene and 196 gm (2 moles) of maleic anhydride is heated with a pan of hot water while butadiene is introduced rapidly (0.6-0.8 liter/min) from a commercial cylinder. The solution is stirred rapidly and the heating is stopped after 3-5 min when the temperature reaches 50°C. In 15-25 min the reaction causes the temperature of the solution to reach 70-75°C. The absorption of the rapid stream of butadiene is nearly complete in 30-40 min. The addition of butadiene is continued at a slower rate for a total of 2\ hr. The solution is poured into a 1-liter beaker which is covered and kept at 0-5°C overnight. The product is collected on a large Buchner funnel and washed with 250 ml of b.p. 35-60°C petroleum ether. A second crop is obtained by diluting the filtrate with an additional 250 ml of petroleum ether. Both crops are dried to constant weight in an oven at 70-80°C to yield 281.5-294.5 gm (96- 97%, m.p. 99-102°C). Recrystallization from ligroin or ether raises the melting point to 103-104°C.
Preparation of Tetrahydrophthalic Anhydride

cis-1,2,3,6-???????????? ?? ?? ? ???

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cis-1,2,3,6-???????????? ?? ??

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