118645-86-6

• 

• Basic information

  1. Product Name: Propanedinitrile, [1-amino-2-(dimethylamino)ethylidene]- (9CI)
  2. Synonyms: Propanedinitrile, [1-amino-2-(dimethylamino)ethylidene]- (9CI)
  3. CAS NO:118645-86-6
  4. Molecular Formula: C7H10N4
  5. Molecular Weight: 150.18
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 118645-86-6.mol
  9. Article Data: 1

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 413.1±45.0 °C(Predicted)
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: 1.112±0.06 g/cm3(Predicted)
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. PKA: 8.12±0.28(Predicted)
  10. CAS DataBase Reference: Propanedinitrile, [1-amino-2-(dimethylamino)ethylidene]- (9CI)(CAS DataBase Reference)
  11. NIST Chemistry Reference: Propanedinitrile, [1-amino-2-(dimethylamino)ethylidene]- (9CI)(118645-86-6)
  12. EPA Substance Registry System: Propanedinitrile, [1-amino-2-(dimethylamino)ethylidene]- (9CI)(118645-86-6)

• 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: 118645-86-6(Hazardous Substances Data)

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118645-86-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 118645-86-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,6,4 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 118645-86:
(8*1)+(7*1)+(6*8)+(5*6)+(4*4)+(3*5)+(2*8)+(1*6)=146
146 % 10 = 6
So 118645-86-6 is a valid CAS Registry Number.

118645-86-6Upstream product

• 124-40-3 dimethyl amine 
• 118645-77-5 2-(1-Amino-chlorethyliden)malondinitril 

118645-86-6Downstream Products

118645-86-6Relevant articles and documents

NEW ONE-POT SYNTHESIS OF ENAMINEDINITRILES

Berry, Robert W. H.,Drewry, Peter C.,Hodson, Harold F.

, p. 958 - 975 (2007/10/02)

A convenient procedure is reported for the one-pot preparation of enaminedinitriles.This involves the sodium methoxide-catalysed addition of methanol to a suitably substituted nitrile followed by reaction of the resulting imidate with malononitrile.The mechanism, scope and limitations of the synthesis have been investigated.Spectroscopic evidence is presented that the products exist in the enaminedinitrile rather than in the tautomeric imino form.Various reactions of the compounds including halogen exchange, anion formation and amine displacement have been studied and used to extend the range of enaminedinitriles prepared.

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