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D28000

Sigma-Aldrich

Diazald®

99%

Synonym(s):

N-Methyl-N-(p-tolylsulfonyl)nitrosamide, N-Methyl-N-nitroso-p-toluenesulfonamide, N-Nitroso-N-methyl-p-toluenesulfonamide, N-Nitroso-p-toluenesulfomethylamide, p-Tolylsulfomethylnitrosamide, Diazomethane precursor

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About This Item

Linear Formula:
CH3C6H4SO2N(CH3)NO
CAS Number:
Molecular Weight:
214.24
Beilstein/REAXYS Number:
2214345
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

99%

form

solid

mp

61-62 °C (lit.)

SMILES string

CN(N=O)S(=O)(=O)c1ccc(C)cc1

InChI

1S/C8H10N2O3S/c1-7-3-5-8(6-4-7)14(12,13)10(2)9-11/h3-6H,1-2H3

InChI key

FFKZOUIEAHOBHW-UHFFFAOYSA-N

Application

Nitrosylating agent for transition metal complexes, amines, and carbanions, as well as a precursor to diazomethane.

Storage and Stability

Warning: these products are subject to the Explosives Act and must be transported refrigerated - additional costs for transport will apply.

Legal Information

Diazald is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

Eye Irrit. 2 - Self-react. C - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

4.1A - Other explosive hazardous materials

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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J. Chem. Soc. Perkin Trans. II, 1233-1233 (1993)
Journal of Chromatographic Science, 29, 8-8 (1991)
J. Chem. Soc. Perkin Trans. II, 29-29 (1993)
Organometallics, 12, 1029-1029 (1993)
Lalit K Golani et al.
Journal of medicinal chemistry, 59(17), 7856-7876 (2016-07-28)
Targeted antifolates with heteroatom replacements of the carbon vicinal to the phenyl ring in 1 by N (4), O (8), or S (9), or with N-substituted formyl (5), acetyl (6), or trifluoroacetyl (7) moieties, were synthesized and tested for selective

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