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17647-57-3

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17647-57-3 Usage

Physical state

Colorless liquid

Odor

Sweet, chloroform-like

Uses

a. Fumigant
b. Pesticide
c. Production of dyes
d. Production of resins
e. Production of pharmaceuticals

Health hazards

a. Skin irritation
b. Eye irritation
c. Respiratory system irritation
d. Prolonged exposure may lead to serious health effects

Safety precautions

Handle and store with caution, follow proper safety procedures when working with it.

Check Digit Verification of cas no

The CAS Registry Mumber 17647-57-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,4 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17647-57:
(7*1)+(6*7)+(5*6)+(4*4)+(3*7)+(2*5)+(1*7)=133
133 % 10 = 3
So 17647-57-3 is a valid CAS Registry Number.

17647-57-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name dichloro(2-methoxyphenyl)methane

1.2 Other means of identification

Product number -
Other names o-methoxybenzylidene chloride

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:17647-57-3 SDS

17647-57-3Upstream product

17647-57-3Relevant articles and documents

Formamide Catalysis Facilitates the Transformation of Aldehydes into Geminal Dichlorides

Huy, Peter Helmut

supporting information, p. 2474 - 2483 (2019/06/08)

Herein, a novel method for the transformation of aldehydes into geminal dichlorides based on phthaloyl chloride as reagent and N -formylpyrrolidine as Lewis base catalyst is disclosed. Given the mild reaction conditions, the current protocol is distinguished by high levels of functional group compatibility and scalability and is operationally simple. The in situ formation of a Vilsmeier Haack reagent type intermediate is likely to be essential for this organocatalytic nucleophilic substitution reaction.

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