Structure of BIS(P-TOLUENESULFONYL)DIAZOMETHANE CAS 14159-45-6

BIS(P-TOLUENESULFONYL)DIAZOMETHANE CAS 14159-45-6

in , , , , , ,

Identification

CAS Number

14159-45-6

Name

BIS(P-TOLUENESULFONYL)DIAZOMETHANE

Synonyms

1,1′-[(Diazomethylen)disulfonyl]bis(4-methylbenzol)
[German]
[IUPAC name – generated by ACD/Name]
1,1′-[(Diazomethylene)disulfonyl]bis(4-methylbenzene)
[IUPAC name – generated by ACD/Name]
1,1′-[(Diazométhylène)disulfonyl]bis(4-méthylbenzène)
[French]
[IUPAC name – generated by ACD/Name]
14159-45-6
[RN]
Benzene, 1,1′-[(diazomethylene)disulfonyl]bis[4-methyl-
[Index name – generated by ACD/Name]
BIS(P-TOLUENESULFONYL)DIAZOMETHANE

SMILES

O=C([O-])c1ccccc1[I+]c1ccccc1

StdInChI

InChI=1S/C13H9IO2/c15-13(16)11-8-4-5-9-12(11)14-10-6-2-1-3-7-10/h1-9H

StdInChIKey

LUGVQQXOGHCZNN-UHFFFAOYSA-N

Molecular Formula

C13H9IO2

Molecular Weight

324.117

MDL number

MFCD04038060

Properties

Appearance

White to off-white powder

Safety Data

RIDADR 

NONH for all modes of transport

WGK Germany

3

Specifications and Other Information of Our BIS(P-TOLUENESULFONYL)DIAZOMETHANE CAS 14159-45-6

Identification Methods

HNMR, HPLC

Purity

99%min, 99.5% min

Total metal impurities

＜100ppb, ＜50ppb

Shelf Life

2 years

Storage

Under room temperature away from light

Known Application

  1. Organic Synthesis Reagent
    It is mainly used as a diazomethane equivalent reagent in organic chemistry. It serves as a mild and safer alternative to diazomethane for:
    Methylation reactions
    Formation of diazo compounds
    Carbenoid-type transformations
  2. Intermediate in Fine Chemical Synthesis
    Used as an intermediate for preparing:
    Sulfonyl-containing compounds
    Functionalized aromatic derivatives
    Specialty organic intermediates for pharmaceuticals and materials
  3. Research & Laboratory Use
    Common in academic and industrial research laboratories for:
    Diazo-transfer reactions
    Mechanistic organic chemistry studies
    Development of new synthetic methodologies involving sulfonyl diazo compounds
  4. Precursor in Chemical Manufacturing
    It can act as a building block for downstream diazo chemistry, including the synthesis of more complex sulfonyl or aryl diazo derivatives.

This product is developed by our R&D company Watson International Ltd (https://www.watson-int.com/).