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100948-84-3

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100948-84-3 Usage

Derivative

Nitrobenzene

Applications

a. Production of pesticides
b. Intermediate in the synthesis of pharmaceuticals

Physical state

Pale yellow solid

Solubility

a. Sparingly soluble in water
b. More soluble in organic solvents

Safety precautions

a. Toxic and potentially harmful to human health
b. Harmful to aquatic organisms
c. Can cause long-term adverse effects in the environment

Check Digit Verification of cas no

The CAS Registry Mumber 100948-84-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,9,4 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 100948-84:
(8*1)+(7*0)+(6*0)+(5*9)+(4*4)+(3*8)+(2*8)+(1*4)=113
113 % 10 = 3
So 100948-84-3 is a valid CAS Registry Number.

100948-84-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-dichloro-4-methoxy-5-nitrobenzene

1.2 Other means of identification

Product number -
Other names 4,5-Dichlor-2-nitro-anisol

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:100948-84-3 SDS

100948-84-3Relevant articles and documents

Preparation of a new chiral building block containing a benzylic quaternary stereogenic center and a formal total synthesis of (-)-physostigmine

Asakawa, Kaori,Noguchi, Naoyoshi,Takashima, Shingo,Nakada, Masahisa

experimental part, p. 2304 - 2309 (2009/04/11)

This paper describes the preparation of a new chiral building block containing a benzylic quaternary stereogenic center via the highly enantioselective PLE-mediated hydrolysis of dimethyl 2-(2-chloro-5-methoxyphenyl)-2-methylmalonate, as well as the absolute configuration of the new chiral building block, which has been elucidated through the formal total synthesis of (-)-physostigmine.

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