15313-46-9

• 

• Basic information

  1. Product Name: m-Chloro-1-cyanoformanilide
  2. Synonyms: m-Chloro-1-cyanoformanilide;N-(3-Chlorophenyl)-1-cyanoformamide
  3. CAS NO:15313-46-9
  4. Molecular Formula: C₈H₅ClN₂O
  5. Molecular Weight: 180.5911
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 15313-46-9.mol
  9. Article Data: 3

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: °Cat760mmHg
  3. Flash Point: °C
  4. Appearance: /
  5. Density: 1.412g/cm³
  6. Refractive Index: 1.627
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: m-Chloro-1-cyanoformanilide(CAS DataBase Reference)
  10. NIST Chemistry Reference: m-Chloro-1-cyanoformanilide(15313-46-9)
  11. EPA Substance Registry System: m-Chloro-1-cyanoformanilide(15313-46-9)

• 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: 15313-46-9(Hazardous Substances Data)

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• SDS
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• Carbonocyanidic amide,(3-chlorophenyl)- (9CI)

  Cas No: 15313-46-9

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• 15313-46-9

  Cas No: 15313-46-9

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• Henan Tianfu Chemical Co., Ltd.
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• Carbonocyanidic amide,(3-chlorophenyl)- (9CI) cas 15313-46-9

  Cas No: 15313-46-9

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15313-46-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15313-46-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,3,1 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15313-46:
(7*1)+(6*5)+(5*3)+(4*1)+(3*3)+(2*4)+(1*6)=79
79 % 10 = 9
So 15313-46-9 is a valid CAS Registry Number.

InChI:InChI=1/C8H5ClN2O/c9-6-2-1-3-7(4-6)11-8(12)5-10/h1-4H,(H,11,12)

15313-46-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name	N-(3-chlorophenyl)-1-cyanoformamide

1.2 Other means of identification

Product number	-
Other names	3-Chlor-oxanilsaeurenitril

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:15313-46-9 SDS

15313-46-9Upstream product

• 85968-59-8 α-Oximino-acetessigsaeure-m-chloranilid 
• 105-56-6 ethyl 2-cyanoacetate 
• 108-42-9 3-chloro-aniline 

15313-46-9Downstream Products

• 17821-33-9 N-(3-Chloro-phenyl)-2-cyano-3,3-bis-methylsulfanyl-acrylamide 

15313-46-9Relevant articles and documents

4,5-Dioxo-imidazolinium Cation Activation of 1-Acyl-1-carbamoyl Oximes: Access to Cyanoformamides Using Dichloroimidazolidinedione

Gao, Yu,Guo, Kai,Guo, Tianfo,Li, Yongqiang,Li, Zhenjiang,Liu, Bo,Yao, Zhiwei,Zhang, Zhihao,Zhu, Yuejia

, (2020/01/31)

Cyanoformamides are prevalent as versatile building blocks for accessing synthetically useful intermediates and biologically active compounds. The development of a milder, simpler, and more efficient approach to cyanoformamides is nontrivial. Herein, we demonstrate the effectiveness of 4,5-dioxo-imidazolinium cation activation for transforming 1-acyl-1-carbamoyl oximes to cyanoformamides. By making use of the readily available and highly modifiable dichloroimidazolidinediones (DCIDs), this novel method of activation offers reactivity remarkably greater than that of other reported protocols, exhibits a high functional group compatibility with mild conditions, and could be scaled up easily. More than 30 examples are demonstrated with good to excellent yields in short reaction times. This research not only provides a mild and efficient alternative approach to assembling a portfolio of cyanoformamides but also extends the dichloroimidazolidinedione-mediated chemistry to encompass the C-C bond cleavage reaction.

Oxanilic acids and derivatives

Baruffini,Borgna,Pagani

, p. 717 - 734 (2007/10/06)

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