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3785-86-2

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3785-86-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3785-86-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,8 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3785-86:
(6*3)+(5*7)+(4*8)+(3*5)+(2*8)+(1*6)=122
122 % 10 = 2
So 3785-86-2 is a valid CAS Registry Number.

3785-86-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (E)-2-cyano-3-[4-(dimethylamino)phenyl]prop-2-enoate

1.2 Other means of identification

Product number -
Other names (E)-methyl 2-cyano-3-(4-(dimethylamino)phenyl)acrylate

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:3785-86-2 SDS

3785-86-2Relevant articles and documents

Facile Method for the Synthesis of Cyanoacrylates by Knoevenagel Condensation

Jonnalagadda, Sreekantha B.,Kerru, Nagaraju,Mabaso, Thabile,Shabalala, Nhlanhla Gracious

, p. 18 - 24 (2021/01/06)

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With the plaque and A β of the nerve fiber entanglement having affinity to the compound and its preparation method

-

Paragraph 0143-0144, (2018/04/26)

The invention provides a compound provided with good affinity and tangled with an Abeta plaque and a nerve fiber. The structural general formula (I) of the compound is as shown in the specification, wherein W is a benzo-hexahydric aromatic ring or a hexah

Microwave synthesis of α-cyano chalcones

Deshpande, Shyam J.,Leger, Paul R.,Sieck, Stephen R.

supporting information; experimental part, p. 1772 - 1775 (2012/05/04)

A novel methodology for facile production of α-cyano chalcones under microwave irradiation is described. Utilizing a Knoevenagel condensation between benzoylacetonitriles and aromatic aldehydes, substituted chalcones are generated via a 15-min, one-pot synthesis. Diversification of aromatic groups, including electron-withdrawing, electron-donating, and heterocyclic substitutions, has led to the isolation of over twenty colored, solid chalcone products. Furthermore the methodology can be extended to the synthesis of benzylidenemalononitriles as well as methyl and ethyl α-cyano cinnamates.

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