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1204-28-0

1204-28-0 Structure

1204-28-0 Structure
IdentificationMore
[Name]

4-Chloroformylphthalic anhydride
[CAS]

1204-28-0
[Synonyms]

1,2,4-BENZENE-TRICARBOXYLIC ACID ANHYDRIDE CHLORIDE
1,2,4-BENZENETRICARBOXYLIC ANHYDRIDE ACID CHLORIDE
1,3-DIOXO-BENZO[C]FURAN-5-CARBOXYLIC ACID CHLORIDE
4-CHLOROFORMYLPHTHALIC ANHYDRIDE
AKOS BBS-00003912
BENZENE-1,2,4-TRICARBOXYLIC 1,2-ANHYDRIDE 4-CHLORIDE
TIMTEC-BB SBB003447
TMAC
TRIMELLITIC ANHYDRIDE ACID CHLORIDE
TRIMELLITIC ANHYDRIDE CHLORIDE
TRIMELLITIC ANHYDRIDE MONO ACID CHLORIDE
1,3-Benzofurandione-5-carbonyl chloride
1,3-dihydro-1,3-dioxo-5-isobenzofurancarbonylchlorid
1,3-Dioxo-1,3-dihydro-2-benzofuran-5-carbonyl chloride
4-(Chlorocarbonyl)phthalic anhydride
4-(Chlorocarboxy)benzenedicarboxylic anhydride
5-Isobenzofurancarbonyl chloride, 1,3-dihydro-1,3-dioxo-
5-Isobenzofurancarbonylchloride,1,3-dihydro-1,3-dioxo-
Anhydrotrimellitic acid chloride
Phthalic anhydride, 4-(chloroformyl)-
[EINECS(EC#)]

214-874-8
[Molecular Formula]

C9H3ClO4
[MDL Number]

MFCD00005924
[Molecular Weight]

210.57
[MOL File]

1204-28-0.mol
Chemical PropertiesBack Directory
[Appearance]

white crystalline solid
[Melting point ]

66-68 °C(lit.)
[Boiling point ]

302.37°C (rough estimate)
[density ]

1.5015 (rough estimate)
[vapor pressure ]

0.017Pa at 20℃
[refractive index ]

1.4571 (estimate)
[storage temp. ]

2-8°C
[solubility ]

soluble in Chloroform
[form ]

powder to lump
[color ]

White to Almost white
[Water Solubility ]

decomposes
[Sensitive ]

Moisture Sensitive
[Detection Methods]

HPLC,NMR
[BRN ]

610823
[InChI]

1S/C9H3ClO4/c10-7(11)4-1-2-5-6(3-4)9(13)14-8(5)12/h1-3H
[InChIKey]

NJMOHBDCGXJLNJ-UHFFFAOYSA-N
[SMILES]

ClC(=O)c1ccc2C(=O)OC(=O)c2c1
[CAS DataBase Reference]

1204-28-0(CAS DataBase Reference)
[NIST Chemistry Reference]

Phthalic , 4-(chloroformyl)-,anhydride(1204-28-0)
[Storage Precautions]

Moisture sensitive
[EPA Substance Registry System]

1204-28-0(EPA Substance)
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)
GHS05
[Signal word ]

Danger
[Hazard statements ]

H314
[Precautionary statements ]

P260-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338-P363
[Hazard Codes ]

C
[Risk Statements ]

R34:Causes burns.
R29:Contact with water liberates toxic gas.
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
[RIDADR ]

UN 3261 8/PG 2
[WGK Germany ]

3
[F ]

10-21
[TSCA ]

Yes
[REACH Registrations]

Active
[HazardClass ]

8
[PackingGroup ]

II
[HS Code ]

29173990
[Storage Class]

8A - Combustible corrosive hazardous materials
[Hazard Classifications]

Eye Dam. 1
Skin Corr. 1B
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

Trimellitic anhydride acid chloride(1204-28-0).msds
Hazard InformationBack Directory
[Chemical Properties]

white crystalline solid
[Uses]

Trimellitic Anhydride Chloride can be used as a reagent to synthesize optical polyamideimides.
[Synthesis Reference(s)]

The Journal of Organic Chemistry, 38, p. 2557, 1973 DOI: 10.1021/jo00954a034
[Flammability and Explosibility]

Notclassified
[Synthesis]

Trimellitic Anhydride

552-30-7

4-Chloroformylphthalic anhydride

1204-28-0

The general procedure for the synthesis of 1,3-dioxo-1,3-dihydroisobenzofuran-5-carbonyl chloride from trimellitic anhydride was as follows: trimellitic anhydride (50 g) and cyclohexane (45 mL) were added to a reaction flask containing 4-dimethylaminopyridine (0.05 g), and heated to 90 °C. Subsequently, thionyl chloride (37.2 g, molar ratio of trimellitic anhydride to thionyl chloride 1:1.2) was added slowly and the reaction mixture was refluxed for 6 hours. Upon completion of the reaction, it was confirmed that no gas was produced. At the end of the reaction, the remaining cyclohexane and excess thionyl chloride were removed by distillation at 90 °C and the solution was recovered at -0.085 MPa. Next, the 180-190 °C fraction was collected by vacuum distillation (vacuum of 750 mmHg) to give trimellitic anhydride chloride (47.6 g). After cooling, the product was a white solid with a melting point of 67.5~68.8 °C, and the HPLC purity was 99.5% in 86.9% yield.

[References]

[1] Patent: CN103626729, 2016, B. Location in patent: Paragraph 0026; 0027
[2] Patent: CN106748963, 2017, A. Location in patent: Paragraph 0048; 0049; 0050; 0051
[3] Patent: CN108341796, 2018, A. Location in patent: Paragraph 0016; 0017; 0018; 0019; 0020; 0021
[4] Patent: US10093929, 2018, B2. Location in patent: Page/Page column 2-3
Spectrum DetailBack Directory
[Spectrum Detail]

4-Chloroformylphthalic anhydride(1204-28-0)1HNMR
4-Chloroformylphthalic anhydride(1204-28-0)Raman
4-Chloroformylphthalic anhydride(1204-28-0)FT-IR
4-Chloroformylphthalic anhydride(1204-28-0)IR
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

Trimellitic anhydride chloride, 98%(1204-28-0)
[TCI AMERICA]

Trimellitic Anhydride Chloride,>98.0%(T)(1204-28-0)
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