1816-89-3

• 

• Basic information

  1. Product Name: 1-(2-oxo-1,2-diphenylethyl)triaza-1,2-dien-2-ium
  2. Synonyms:
  3. CAS NO:1816-89-3
  4. Molecular Formula: C₁₄H₁₁N₃O
  5. Molecular Weight: 238.264
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 1816-89-3.mol
  9. Article Data: 9

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: N/A
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: 1-(2-oxo-1,2-diphenylethyl)triaza-1,2-dien-2-ium(CAS DataBase Reference)
  10. NIST Chemistry Reference: 1-(2-oxo-1,2-diphenylethyl)triaza-1,2-dien-2-ium(1816-89-3)
  11. EPA Substance Registry System: 1-(2-oxo-1,2-diphenylethyl)triaza-1,2-dien-2-ium(1816-89-3)

• 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: 1816-89-3(Hazardous Substances Data)

• Suppliers
• Usage
• SDS
• Upstream product
• Downstream Products
• Article

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• Ethanone,2-azido-1,2-diphenyl-

  Cas No: 1816-89-3

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• CAS1816-89-3 2-azido-1,2-diphenylethanone

  Cas No: 1816-89-3

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• Ethanone,2-azido-1,2-diphenyl- cas 1816-89-3

  Cas No: 1816-89-3

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1816-89-3 Usage

Chemical structure

1-(2-oxo-1,2-diphenylethyl)triaza-1,2-dien-2-ium is a complex chemical compound with a triaza-1,2-dien-2-ium core and a 1-(2-oxo-1,2-diphenylethyl) group attached.

Field of interest

It is of interest in the field of organic chemistry due to its unique structure and potential applications.

Potential applications

It may have potential applications in various chemical processes and reactions, although further research and testing are necessary to fully understand its properties and uses.

Further research

Additional research and testing may be necessary to fully understand the properties, potential uses, and any possible side effects or hazards associated with 1-(2-oxo-1,2-diphenylethyl)triaza-1,2-dien-2-ium.

Check Digit Verification of cas no

The CAS Registry Mumber 1816-89-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,1 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1816-89:
(6*1)+(5*8)+(4*1)+(3*6)+(2*8)+(1*9)=93
93 % 10 = 3
So 1816-89-3 is a valid CAS Registry Number.

1816-89-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name	2-azido-1,2-diphenylethanone

1.2 Other means of identification

Product number	-
Other names	2-azido-1,2-diphenyl-ethanone

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:1816-89-3 SDS

1816-89-3Upstream product

• 87119-38-8 2-<(4-Nitrobenzenesulfonyl)oxy>-1,2-diphenylethanone 
• 451-40-1 phenyl benzyl ketone 
• 88089-52-5 (Z)-((1,2-diphenylvinyl)oxy)trimethylsilane 
• 119-53-9 2-hydroxy-2-phenylacetophenone 
• 103-30-0 (E)-1,2-diphenyl-ethene 
• 447-31-4 Desyl chloride 
• 588-59-0 stilbene 

1816-89-3Downstream Products

• 71559-19-8 5,7,8-triphenyl-1,4,6-trioxa-9-aza-5λ⁵-phospha-spiro[4.4]non-7-ene 
• 5533-73-3 4,5-Diphenyl-1H-[1,2,3]triazole 
• 5496-31-1 2-(4-methylphenyl)-4,5-diphenyl-1H-imidazole 
• 451-40-1 phenyl benzyl ketone 
• 100-52-7 benzaldehyde 
• 100-47-0 benzonitrile 
• 51608-62-9 (E)-N-benzylidenebenzamide 
• 71559-20-1 2,3,5-triphenyl-1,6,10-trioxa-4-aza-5λ⁵-phospha-spiro[4.5]dec-2-ene 

1816-89-3Relevant articles and documents

-

Ehrenfreund,J.,Zbiral,E.

, p. 1697 - 1704 (1972)

-

Method for preparing alpha-azidoketone compounds based on photocatalysis

-

Paragraph 0186; 0187; 0188, (2018/10/11)

The invention discloses a method for preparing alpha-azidoketone compounds based on photocatalysis. The method is based on a reaction formula shown in the description, wherein R is optionally-substituted aryl, heteroaryl or 1-12 carbon alkyl; R is o

Visible-light-enabled oxyazidation of alkenes leading to α-azidoketones in air

Wei, Wei,Cui, Huanhuan,Yue, Huilan,Yang, Daoshan

supporting information, p. 3197 - 3202 (2018/07/29)

A new and facile visible-light-enabled method for the synthesis of α-azidoketones has been developed via oxyazidation of alkenes with TMSN3 in air at room temperature. A series of α-azidoketones could be easily and efficiently obtained in moder

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