2,4-Dichlorobenzenediazonium 1,5-naphthalenedisulfonate hydrate CAS 123333-91-5

2,4-Dichlorobenzenediazonium 1,5-naphthalenedisulfonate hydrate CAS 123333-91-5

Identification

CAS Number

123333-91-5

Name

2,4-Dichlorobenzenediazonium 1,5-naphthalenedisulfonate hydrate

Synonyms

123333-91-5 [RN]
2,4-DCPD
2,4-Dichlorbenzoldiazonium-5-sulfo-1-naphthalinsulfonathydrat (1:1:1) [German] [ACD/IUPAC Name]
2,4-Dichlorobenzenediazonium 5-sulfo-1-naphthalenesulfonate hydrate (1:1:1) [ACD/IUPAC Name]
2,4-Dichlorophenyldiazonium 1,5-naphthalenedisulfonate
5-Sulfo-1-naphtalènesulfonate de 2,4-dichlorobenzènediazonium, hydrate (1:1:1) [French] [ACD/IUPAC Name]
MFCD08457580 [MDL number]
2,4-Dichlorobenzenediazonium 1,5-naphthalenedisulfonate hydrate
2,4-dichlorobenzenediazonium;5-sulfonaphthalene-1-sulfonate;hydrate
Validated by Experts, Validated by Users, Non-Validated, Removed by Users

SMILES

c1cc2c(cccc2S(=O)(=O)[O-])c(c1)S(=O)(=O)O.c1cc(c(cc1Cl)Cl)[N+]#N.O

StdInChI

InChI=1S/C10H8O6S2.C6H3Cl2N2.H2O/c11-17(12,13)9-5-1-3-7-8(9)4-2-6-10(7)18(14,15)16;7-4-1-2-6(10-9)5(8)3-4;/h1-6H,(H,11,12,13)(H,14,15,16);1-3H;1H2/q;+1;/p-1

StdInChIKey

SPGAUZWLXGQOLT-UHFFFAOYSA-M

Molecular Formula

C16H12Cl2N2O7S2

Molecular Weight

479.312

MDL Number

MFCD08457580

Properties

Appearance

Faint Yellow to Yellow to Beige and Faint Brown to Light Brown to Light Orange powder

Safety Data

Symbol

exclamation-mark-jpgGHS07

Signal Word

Warning

Hazard statements

H315-H319-H335

Precautionary Statements

P261 – P264 – P271 – P280 – P302 + P352 – P305 + P351 + P338

WGK Germany

3

MSDS Download

Specifications and Other Information of Our

Identification Methods

Purity

97% min

Shelf Life

Storage

Store at 2~8° for long time.

Known Application

2,4-Dichlorobenzenediazonium 1,5-naphthalenedisulfonate hydrate CAS 123333-91-5 is used a intermediates. 1,5-Naphthalenedisulfonic acid salt hydrate is a coordination compound commonly used as a reagent or intermediate in organic synthesis. It can be employed in the synthesis of pharmaceuticals, dyes, polymers, and other organic compounds. In the laboratory, it can also serve as a catalyst or precursor to catalysts in organic synthesis reactions.

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