99863-12-4

• 

• Basic information

  1. Product Name: Piperidine, 6-isopropyl-2,2-dimethyl- (6CI)
  2. Synonyms: Piperidine, 6-isopropyl-2,2-dimethyl- (6CI)
  3. CAS NO:99863-12-4
  4. Molecular Formula: C10H21N
  5. Molecular Weight: 155.28044
  6. EINECS: N/A
  7. Product Categories: ISOPROPYL
  8. Mol File: 99863-12-4.mol
  9. Article Data: 1

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: Piperidine, 6-isopropyl-2,2-dimethyl- (6CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: Piperidine, 6-isopropyl-2,2-dimethyl- (6CI)(99863-12-4)
  11. EPA Substance Registry System: Piperidine, 6-isopropyl-2,2-dimethyl- (6CI)(99863-12-4)

• 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: 99863-12-4(Hazardous Substances Data)

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99863-12-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99863-12-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,8,6 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 99863-12:
(7*9)+(6*9)+(5*8)+(4*6)+(3*3)+(2*1)+(1*2)=194
194 % 10 = 4
So 99863-12-4 is a valid CAS Registry Number.

99863-12-4Upstream product

• 1116651-59-2 (S)-2,7-dimethyloct-7-en-3-amine 
• 1116651-82-1 (R)-2,7-dimethyloct-7-en-3-amine 

99863-12-4Downstream Products

99863-12-4Relevant articles and documents

Asymmetric synthesis of α-alkylated aldehydes using terminal epoxide-derived chiral enamines

Hodgson, David M.,Kaka, Naeem S.

supporting information; experimental part, p. 9958 - 9960 (2009/06/30)

(Chemical Equation Presented) Effective discrimination: Efficient lithium amide-induced terminal epoxide-enamine transformation provides the first enamines capable of generating α-alkylated aldehydes with high asymmetric induction by intermolecular nucleophilic substitution (see scheme).

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