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2388-58-1

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2388-58-1 Usage

Appearance

Yellow, crystalline solid

Usage

Commonly used as a reagent in organic synthesis

Classification

Nitroaromatic compound (contains nitro groups and an aromatic ring)

Chemical property

Powerful electrophilic character

Applications

Useful in chemical reactions for the synthesis of dyes and pharmaceuticals

Potential use

Studied for its potential use as an explosive or propellant due to its relatively high energy content

Safety concerns

Toxic and poses health hazards with prolonged exposure

Handling and storage

Should be handled and stored with caution

Check Digit Verification of cas no

The CAS Registry Mumber 2388-58-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,8 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2388-58:
(6*2)+(5*3)+(4*8)+(3*8)+(2*5)+(1*8)=101
101 % 10 = 1
So 2388-58-1 is a valid CAS Registry Number.

2388-58-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethoxysulfanyl-2,4-dinitrobenzene

1.2 Other means of identification

Product number -
Other names 2,4-dinitro-benzenesulfenic acid ethyl 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:2388-58-1 SDS

2388-58-1Relevant articles and documents

Influence of trimethylsilyl substituents on primary C-O bond lengths at the β-position: Results from low-temperature x-ray structural studies

Green, Alison J.,Issa, William,White, Jonathan M.

, p. 927 - 932 (2007/10/03)

The β-trimethylsilyl substituent in 2-trimethylsilylethyl p-nitrobenzoate (12b) and 2-trimethylsilylethyl 2,4-dinitrobenzenesulfenate (12c) leads to significant lengthening of the C(alkyl)-O(ester) bond. Lengthening of the Si-CH2 distance in the more electronegative ester (12c) relative to (12b) is also observed. These structural effects are consistent with the presence of σ C-Si-σ* C-O interactions.

REACTION OF THIOSULFONIC ESTERS WITH CYANOACETIC ESTER IN THE PRESENCE OF ALCOHOLATES

Bilozor, T.K.,Boldyrev, B.G.

, p. 807 - 808 (2007/10/02)

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