1,2,3,6-tetrahydrophthalimide (CAS 85-40-5) — formula C8H9NO2, molecular weight 151.16; category organic chemicals.
| CAS Number | 85-40-5 |
|---|---|
| Molecular Formula | C8H9NO2 |
| Molecular Weight | 151.16 |
| Melting Point | 137 °C |
| LogP | 0.2 |
| Applications | Uses: Used as a chemical intermediate for the fungicides Captan and Captafol, [HSDB], Captan is produced by reaction of 1, 2, 3, 6-tetrahydrophthalimide with trichloromethanesulfenyl chloride (perchloromethylmercaptan) in the presence of sodium hydroxide., CHEM INT FOR PESTICIDES (EG, CAPTAN AND CAPTAFOL), Use Classification: Transformation products, Environmental transformation -> Pesticide transformation products (metabolite, successor), Methods of Manufacturing: REACTION OF TETRACHLOROPHTHALIC ANHYDRIDE WITH AMMONIA, Consumption Patterns: ESSENTIALLY 100% AS A CHEMICAL INTERMEDIATE, U.S. Production: (1977) PROBABLY GREATER THAN 2.27X10+6 GRAMS, (1979) PROBABLY GREATER THAN 2.27X10+6 GRAMS, 1H-Isoindole-1, 3(2H)-dione, 3a, 4, 7, 7a-tetrahydro- is listed as a High Production Volume (HPV) chemical (65FR81686). Chemicals listed as HPV were produced in or imported into the U.S. in >1 million pounds in 1990 and, or 1994. The HPV list is based on the 1990 Inventory Update Rule. (IUR) (40 CFR part 710 subpart B, 51FR21438)., Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#4998], U.S. Imports: (1977) No Data, (1979) No Data, U.S. Exports: (1977) No Data, General Manufacturing Information: 1H-Isoindole-1, 7a-tetrahydro-: ACTIVE, A method for destruction of captan usuitable for use is discussed. Captan was decomposed to nontoxic tetrahydrophthalimide.. |
| Category | Organic Chemicals |
Documented applications: Uses: Used as a chemical intermediate for the fungicides Captan and Captafol, [HSDB], Captan is produced by reaction of 1, 2, 3, 6-tetrahydrophthalimide with trichloromethanesulfenyl chloride (perchloromethylmercaptan) in the presence of sodium hydroxide., CHEM INT FOR PESTICIDES (EG, CAPTAN AND CAPTAFOL), Use Classification: Transformation products, Environmental transformation -> Pesticide transformation products (metabolite, successor), Methods of Manufacturing: REACTION OF TETRACHLOROPHTHALIC ANHYDRIDE WITH AMMONIA, Consumption Patterns: ESSENTIALLY 100% AS A CHEMICAL INTERMEDIATE, U.S. Production: (1977) PROBABLY GREATER THAN 2.27X10+6 GRAMS, (1979) PROBABLY GREATER THAN 2.27X10+6 GRAMS, 1H-Isoindole-1, 3(2H)-dione, 3a, 4, 7, 7a-tetrahydro- is listed as a High Production Volume (HPV) chemical (65FR81686). Chemicals listed as HPV were produced in or imported into the U.S. in >1 million pounds in 1990 and, or 1994. The HPV list is based on the 1990 Inventory Update Rule. (IUR) (40 CFR part 710 subpart B, 51FR21438)., Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#4998], U.S. Imports: (1977) No Data, (1979) No Data, U.S. Exports: (1977) No Data, General Manufacturing Information: 1H-Isoindole-1, 7a-tetrahydro-: ACTIVE, A method for destruction of captan usuitable for use is discussed. Captan was decomposed to nontoxic tetrahydrophthalimide...
1,2,3,6-tetrahydrophthalimide is a carbon-based organic compound with CAS registry number 85-40-5 and molecular formula C8H9NO2 (molecular weight 151.16), belonging to the organic chemicals segment of chemical raw materials.
CAS number: 85-40-5
Its molecular formula C8H9NO2 comprises 8 C, 9 H, 1 N, 2 O atoms.
Also known as: 1,2,3,6-tetrahydrophthalimide · 1,2,3,6-四氢邻苯二甲酰亚胺
Category: organic chemicals
The CAS registry number of 1,2,3,6-tetrahydrophthalimide is 85-40-5.
Molecular formula C8H9NO2, molecular weight 151.16.
It is also registered under: 1,2,3,6-tetrahydrophthalimide, 1,2,3,6-四氢邻苯二甲酰亚胺.
Recorded applications: Uses: Used as a chemical intermediate for the fungicides Captan and Captafol, [HSDB], Captan is produced by reaction of 1, 2, 3, 6-tetrahydrophthalimide with trichloromethanesulfenyl chloride (perchloromethylmercaptan) in the presence of sodium hydroxide., CHEM INT FOR PESTICIDES (EG, CAPTAN AND CAPTAFOL), Use Classification: Transformation products, Environmental transformation -> Pesticide transformation products (metabolite, successor), Methods of Manufacturing: REACTION OF TETRACHLOROPHTHALIC ANHYDRIDE WITH AMMONIA, Consumption Patterns: ESSENTIALLY 100% AS A CHEMICAL INTERMEDIATE, U.S. Production: (1977) PROBABLY GREATER THAN 2.27X10+6 GRAMS, (1979) PROBABLY GREATER THAN 2.27X10+6 GRAMS, 1H-Isoindole-1, 3(2H)-dione, 3a, 4, 7, 7a-tetrahydro- is listed as a High Production Volume (HPV) chemical (65FR81686). Chemicals listed as HPV were produced in or imported into the U.S. in >1 million pounds in 1990 and, or 1994. The HPV list is based on the 1990 Inventory Update Rule. (IUR) (40 CFR part 710 subpart B, 51FR21438)., Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#4998], U.S. Imports: (1977) No Data, (1979) No Data, U.S. Exports: (1977) No Data, General Manufacturing Information: 1H-Isoindole-1, 7a-tetrahydro-: ACTIVE, A method for destruction of captan usuitable for use is discussed. Captan was decomposed to nontoxic tetrahydrophthalimide...
Category: Organic Chemicals.
Independent reference data for 1,2,3,6-tetrahydrophthalimide (CAS 85-40-5), compiled from public chemistry databases.
| CAS Registry Number | 85-40-5 |
|---|---|
| PubChem CID | 6808 |
| Molecular formula | C8H9NO2 |
| IUPAC name | 3a,4,7,7a-tetrahydroisoindole-1,3-dione |
| Molecular Weight | 151.16 |
|---|---|
| XLogP3 | 0.2 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | 151.063328530 |
| Monoisotopic Mass | 151.063328530 |
| Topological Polar Surface Area | 46.2 |
| Heavy Atom Count | 11 |
| Melting Point | 137 °C |
|---|---|
| Flash Point | 190 °C |
85-40-5; 1,2,3,6-TETRAHYDROPHTHALIMIDE; 4-Cyclohexene-1,2-dicarboximide; Tetrahydrophthalic acid imide; 1H-Isoindole-1,3(2H)-dione, 3a,4,7,7a-tetrahydro-; delta(4)-Tetrahydrophthalimide; DTXSID8026513; delta(sup 4)-Tetrahydrophthalimide; NSC 59011; CCRIS 3648; HSDB 5006; EINECS 201-602-8; Isoindole-1,3-dione, 3a,4,7,7a-tetrahydro-; BRN 0128764; DTXCID106513; EC 201-602-8
1,2,3,6-tetrahydrophthalimide · CAS 85-40-5 · C8H9NO2. Melting Point: 137 °C; Flash Point: 190 °C.
Source: PubChem / Wikidata; the batch COA governs where values differ.
Supplier: Jinan Shenghe Chemical Co., Ltd.
中文页面: 1,2,3,6-四氢邻苯二甲酰亚胺