133973-80-5

• 

• Basic information

  1. Product Name: 2,7-dihydro-7-phenyl-2-(phenylmethyl)-5-propoxy-3H-imidazo(1,2-c)pyrazolo(4,3-e)pyrimidine
  2. Synonyms: 2,7-dihydro-7-phenyl-2-(phenylmethyl)-5-propoxy-3H-imidazo(1,2-c)pyrazolo(4,3-e)pyrimidine
  3. CAS NO:133973-80-5
  4. Molecular Formula: C23H23 N5 O
  5. Molecular Weight: 0
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 133973-80-5.mol
  9. Article Data: 2

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 554.3°Cat760mmHg
  3. Flash Point: 289°C
  4. Appearance: /
  5. Density: 1.27g/cm³
  6. Vapor Pressure: 2.5E-12mmHg at 25°C
  7. Refractive Index: 1.681
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 2,7-dihydro-7-phenyl-2-(phenylmethyl)-5-propoxy-3H-imidazo(1,2-c)pyrazolo(4,3-e)pyrimidine(CAS DataBase Reference)
  11. NIST Chemistry Reference: 2,7-dihydro-7-phenyl-2-(phenylmethyl)-5-propoxy-3H-imidazo(1,2-c)pyrazolo(4,3-e)pyrimidine(133973-80-5)
  12. EPA Substance Registry System: 2,7-dihydro-7-phenyl-2-(phenylmethyl)-5-propoxy-3H-imidazo(1,2-c)pyrazolo(4,3-e)pyrimidine(133973-80-5)

• 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: 133973-80-5(Hazardous Substances Data)

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• SDS
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• Downstream Products
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• 2,7-DIHYDRO-7-PHENYL-2-BENZYL-5-PROPOXY-3H-IMIDAZO[1,2-C]PYRAZOLO(4,3-E)PYRIMIDINE

  Cas No: 133973-80-5

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133973-80-5 Usage

Heterocyclic compound

Contains a fused imidazo-pyrazolo-pyrimidine ring system

Side chains

Phenylmethyl and propoxy attached to nitrogen and carbon atoms, respectively

Potential pharmacological properties

Studied as a ligand for various receptors and enzymes

Interest for further research

Unique structure and properties make it a potential candidate for medicinal chemistry and drug development applications

Check Digit Verification of cas no

The CAS Registry Mumber 133973-80-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,9,7 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 133973-80:
(8*1)+(7*3)+(6*3)+(5*9)+(4*7)+(3*3)+(2*8)+(1*0)=145
145 % 10 = 5
So 133973-80-5 is a valid CAS Registry Number.

InChI:InChI=1/C23H23N5O/c1-2-13-29-23-26-22-20(15-24-28(22)19-11-7-4-8-12-19)21-25-18(16-27(21)23)14-17-9-5-3-6-10-17/h3-12,15,18H,2,13-14,16H2,1H3

133973-80-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name	133973-80-5

1.2 Other means of identification

Product number	-
Other names	Dppipp,(S(-))

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:133973-80-5 SDS

133973-80-5Upstream product

• 133973-87-2 (S)-2,7-dihydro-7-phenyl-2-(phenylmethyl)-5-chloro-3H-imidazo<1,2-c>pyrazolo<4,3-e>pyrimidine 
• 132537-82-7 (S)-β-<(1-phenyl-6-chloro-1H-pyrazolo<3,4-d>pyrimidin-4-yl)amino>benzenepropanol 
• 99971-84-3 4,6-dichloro-1-phenyl-1H-pyrazolo<3,4-d>pyrimidine 
• 3182-95-4 L-Phenylalaninol 
• 6819-41-6 sodium n-propoxide 
• 132537-83-8 (R)-β-<(1-phenyl-6-chloro-1H-pyrazolo<3,4-d>pyrimidin-4-yl)amino>benzenepropanol 
• 5267-64-1 (R)-2-amino-3-phenylpropanol 
• 142613-27-2 (RS)-2,7-dihydro-7-phenyl-2-(phenylmethyl)-5-chloro-3H-imidazo<1,2-c>pyrazolo<4,3-e>pyrimidine 

133973-80-5Downstream Products

133973-80-5Relevant articles and documents

Conformationally restrained, chiral (phenylisopropyl)amino-substituted pyrazolo[3,4-d]pyrimidines and purines with selectivity for adenosine A1 and A2 receptors

Peet,Lentz,Sunder,Dudley,Ogden

, p. 3263 - 3269 (2007/10/02)

Two modes of tethering a chiral (phenylisopropyl)amino substituent in pyrazolo[3,4-d]pyrimidines and purines have been explored. One mode gave (S)- 2,7-dihydro-7-phenyl-2-(phenylmethyl)-5-propoxy-3H-imidazo[1,2-c]pyrazolo- [4,3-e]pyrimidine (12a) and its corresponding R-enantiomer 12b, which were selective for A2 and A1 adenosine receptors, respectively. The corresponding diimidazo[1,2-c:4',5'-e]pyrimidines 12e and 12f were analogously selective. This is the first example where a single chiral recognition unit provides enantiomers with opposite selectivities for adenosine receptors. The second mode gave (2S-trans)-2,7-dihydro-2-methyl- 3,7-diphenyl-5-propoxy-3H-imidazo[1,2-c]-pyrazolo[4,3-e]pyrimidine (12c) and its corresponding R-enantiomer 12d. Compounds 12c and 12d were significantly less potent than 12a and 12b at A1 receptors, and were nonselective.

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