1101-39-9

• 

• Basic information

  1. Product Name: tetramethyl 4H-quinolizine-1,2,3,4-tetracarboxylate
  2. Synonyms: Tetramethyl 4H-quinolizine-1,2,3,4-tetracarboxylate
  3. CAS NO:1101-39-9
  4. Molecular Formula: C₁₇H₁₇NO₈
  5. Molecular Weight: 363.3188
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 1101-39-9.mol
  9. Article Data: 3

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 497.9°C at 760 mmHg
  3. Flash Point: 254.9°C
  4. Appearance: N/A
  5. Density: 1.38g/cm³
  6. Vapor Pressure: 4.74E-10mmHg at 25°C
  7. Refractive Index: 1.573
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: tetramethyl 4H-quinolizine-1,2,3,4-tetracarboxylate(CAS DataBase Reference)
  11. NIST Chemistry Reference: tetramethyl 4H-quinolizine-1,2,3,4-tetracarboxylate(1101-39-9)
  12. EPA Substance Registry System: tetramethyl 4H-quinolizine-1,2,3,4-tetracarboxylate(1101-39-9)

• 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: 1101-39-9(Hazardous Substances Data)

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• SDS
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• Downstream Products
• Article

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• 4H-Quinolizine-1,2,3,4-tetracarboxylicacid, 1,2,3,4-tetramethyl ester

  Cas No: 1101-39-9

• USD $ 3.0-3.0 / Kilogram

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• 1101-39-9

  Cas No: 1101-39-9

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• Henan Tianfu Chemical Co., Ltd.
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• 4H-Quinolizine-1,2,3,4-tetracarboxylicacid, 1,2,3,4-tetramethyl ester cas 1101-39-9

  Cas No: 1101-39-9

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1101-39-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1101-39-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,0 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1101-39:
(6*1)+(5*1)+(4*0)+(3*1)+(2*3)+(1*9)=29
29 % 10 = 9
So 1101-39-9 is a valid CAS Registry Number.

1101-39-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name	tetramethyl 4H-quinolizine-1,2,3,4-tetracarboxylate

1.2 Other means of identification

Product number	-
Other names	4H-quinolizin-1,2,3,4-tetracarboxylic acid tetramethyl ester

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:1101-39-9 SDS

1101-39-9Upstream product

• 110-86-1 pyridine 
• 623-73-4 diazoacetic acid ethyl ester 
• 762-42-5 dimethyl acetylenedicarboxylate 
• 13737-04-7 2-(trimethylsilyl)pyridine 
• 101878-66-4 tetramethyl 9aH-quinolizine-1,2,3,4-tetracarboxylate 
• 75-05-8 acetonitrile 
• 64-19-7 acetic acid 
• 67-56-1 methanol 
• 60-29-7 diethyl ether 

1101-39-9Downstream Products

• 115-10-6 Dimethyl ether 
• 79-20-9 acetic acid methyl ester 
• 18782-33-7 3-(Methoxycarbonylmethyl)-1,2-indolizindicarbonsaeure-dimethylester 
• 4491-43-4 1,2,3-Indolizintricarbonsaeure-trimethylester 
• 16959-60-7 1,2-Indolizindicarbonsaeure-dimethylester 
• 82884-77-3 2,3-Indolizindicarbonsaeure-dimethylester 

1101-39-9Relevant articles and documents

Iron-Catalyzed Indolizine Synthesis from Pyridines, Diazo Compounds, and Alkynes

Douglas, Tim,Pordea, Anca,Dowden, James

, p. 6396 - 6399 (2017)

The iron(III)-catalyzed synthesis of indolizines from commercially available alkyne, pyridine, and diazo precursors is reported. This mild, expedient method is tolerant of various solvents and proceeds with as little as 0.25 mol % [Fe(TPP)Cl]. Significant

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Acheson,Hole

, p. 748,752 (1962)

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