89877-62-3

• 

• Basic information

  1. Product Name: 6-Cyanophthalide
  2. Synonyms: 1,3-Dihydro-1-oxoisobenzofuran-6-carbonitrile;3-oxo-1,3-dihydro-2-benzofuran-5-carbonitrile;3-Oxo-1,3-dihydroisobenzofuran-5-carbonitrile
  3. CAS NO:89877-62-3
  4. Molecular Formula: C₉H₅NO₂
  5. Molecular Weight: 159.1415
  6. EINECS: 604-604-1
  7. Product Categories: Aromatics;Miscellaneous Reagents
  8. Mol File: 89877-62-3.mol

• Chemical Properties

  1. Melting Point: 193-195°C
  2. Boiling Point: 391.03°C at 760 mmHg
  3. Flash Point: 190.046°C
  4. Appearance: /
  5. Density: 1.36g/cm³
  6. Vapor Pressure: 0mmHg at 25°C
  7. Refractive Index: 1.607
  8. Storage Temp.: -20°C Freezer, Under Inert Atmosphere
  9. Solubility: N/A
  10. CAS DataBase Reference: 6-Cyanophthalide(CAS DataBase Reference)
  11. NIST Chemistry Reference: 6-Cyanophthalide(89877-62-3)
  12. EPA Substance Registry System: 6-Cyanophthalide(89877-62-3)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 89877-62-3(Hazardous Substances Data)

• Suppliers
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• SDS
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• Article

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• 6-Cyanophthalide

  Cas No: 89877-62-3

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• Amadis Chemical Co., Ltd.
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• 3-OXO-1,3-DIHYDROISOBENZOFURAN-5-CARBONITRILE

  Cas No: 89877-62-3

• USD $ 3.0-3.0 / Kilogram

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• 5-Isobenzofurancarbonitrile,1,3-dihydro-3-oxo-

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• Hangzhou J&H Chemical Co., Ltd.
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• 3-OXO-1,3-DIHYDROISOBENZOFURAN-5-CARBONITRILE

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89877-62-3 Usage

Chemical Properties

White Solid

Uses

6-Cyanophthalide can be used as a useful synthetic intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 89877-62-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,8,7 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 89877-62:
(7*8)+(6*9)+(5*8)+(4*7)+(3*7)+(2*6)+(1*2)=213
213 % 10 = 3
So 89877-62-3 is a valid CAS Registry Number.

InChI:InChI=1/C9H5NO2/c10-4-6-1-2-7-5-12-9(11)8(7)3-6/h1-3H,5H2

89877-62-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	3-oxo-1H-2-benzofuran-5-carbonitrile

1.2 Other means of identification

Product number	-
Other names	3-oxo-phthalan-5-carbonitrile

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:89877-62-3 SDS

89877-62-3Upstream product

• 1446757-51-2 3,4-bis(hydroxymethyl)benzonitrile 

89877-62-3Downstream Products

• 1231890-89-3 N-(3-bromo-2-methylphenyl)-5-cyano-2-(hydroxymethyl)benzamide 
• 1379192-20-7 C₉H₇NO₃ 

89877-62-3Relevant articles and documents

Facile organocatalytic domino oxidation of diols to lactones by in situ-generated TetMe-IBX

Jhulki, Samik,Seth, Saona,Mondal, Manas,Moorthy, Jarugu Narasimha

, p. 2286 - 2293 (2014/03/21)

The domino oxidation of diols to lactones is an important transformation, and catalytic protocols that allow this conversion smoothly are scarce. Capitalizing on the established reactivity of tetramethyl-IBX (TetMe-IBX) and its in situ generation in the presence of a co-oxidant, such as oxone, we have shown that a variety of diols can be converted to the corresponding lactones in respectable yields by employing the precursor of TetMe-IBX, namely, tetramethyl-o-iodobenzoic acid (TetMe-IA), as a catalyst in 5 mol % in the presence of 2 equiv of oxone.

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