| Identification | Back Directory | [Name]
Phthalylglycyl chloride | [CAS]
6780-38-7 | [Synonyms]
NSC 401729
PHTHALYL-GLYCYL CHLORIDE
N-Phthalylglycyl chloride
Phthalylglycyl chloride 96%
Phthalylglycine acid chloride
N,N-Phthaloylglycine chloride
Phthalyl-glycyl chloride ,98%
2-(Phthalimidyl)acetyl chloride
2-Phthalimidylacetic acid chloride
N-(2-Chloro-2-oxoethyl)phthalimide
1,3-Dioxo-2-isoindolineacetyl chloride
2-(1,3-dioxoisoindol-2-yl)acetyl chloride
2-(1,3-dioxoisoindol-2-yl)ethanoyl chloride
2-(1,3-dioxo-2-isoindolinyl)acetyl chloride
2-(1,3-dioxoisoindolin-2-yl)
acetyl chloride
2-(1,3-diketoisoindolin-2-yl)acetyl chloride
(1,3-Dioxo-2H-isoindole-2-yl)acetyl chloride
1,3-dihydro-1,3-dioxo-2h-isoindole-2-acetylchlorid
1,3-dihydro-1,3-dioxo-2H-isoindole-2-acetyl chloride
N-Phthalylglycyl chloride(Phthalimide acetyl chloride)
2H-Isoindole-2-acetyl chloride, 1,3-dihydro-1,3-dioxo-
(1,3-Dioxo-1,3-dihydro-2H-isoindol-2-yl)acetyl chloride
1,3-Dihydro-1,3-dioxo-2H-isoindole-2-acetic acid chloride | [EINECS(EC#)]
229-840-8 | [Molecular Formula]
C10H6ClNO3 | [MDL Number]
MFCD00192872 | [MOL File]
6780-38-7.mol | [Molecular Weight]
223.61 |
| Chemical Properties | Back Directory | [Appearance]
slight yellow to white crystalline powder | [Melting point ]
84-85 °C | [Boiling point ]
190-192 °C(Press: 15 Torr) | [density ]
1.504±0.06 g/cm3(Predicted) | [storage temp. ]
Inert atmosphere,Store in freezer, under -20°C | [solubility ]
Chloroform, Dichloromethane | [form ]
Solid | [pka]
-2.56±0.20(Predicted) | [color ]
White | [InChI]
1S/C10H6ClNO3/c11-8(13)5-12-9(14)6-3-1-2-4-7(6)10(12)15/h1-4H,5H2 | [InChIKey]
RHZBRCQIKQUQHQ-UHFFFAOYSA-N | [SMILES]
ClC(=O)CN1C(=O)c2ccccc2C1=O |
| Hazard Information | Back Directory | [Chemical Properties]
slight yellow to white crystalline powder | [Uses]
Reactant involved in:• ;Synthesis of selenium-containing amino acid analogs with bactericidal and antifungal activity1• ;Photoinduced single electron transfer cyclization for preparation of cyclic peptides2• ;Arndt-Eistert synthesis3• ;Mitsunobu and arbuzov-type multicomponent pathway4• ;Remote C-H bond functionalization5• ;Amido-alkylation for synthesis of benzofuran derivatives6 | [General Description]
Phthalylglycyl chloride can be synthesized via reaction of phthalyl-glycine with thionyl chloride. |
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| Company Name: |
J & K SCIENTIFIC LTD.
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18210857532 18210857532 |
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https://www.jkchemical.com |
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Energy Chemical
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400-0056266 |
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www.energy-chemical.com |
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Sigma-Aldrich
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021-61415566 800-8193336 |
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https://www.sigmaaldrich.cn |
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DebyeTec.com Inc.
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skychemical Co.Ltd
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021-20960837,QQ1332204249 |
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http://www.skychemical.com |
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