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Acetamide, N-3-butenyl-2,2,2-trifluoro-N-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

233590-33-5

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233590-33-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 233590-33-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,3,5,9 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 233590-33:
(8*2)+(7*3)+(6*3)+(5*5)+(4*9)+(3*0)+(2*3)+(1*3)=125
125 % 10 = 5
So 233590-33-5 is a valid CAS Registry Number.

233590-33-5SDS

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 N-benzyl-N-(but-3-enyl)-2,2,2-trifluoroacetamide

1.2 Other means of identification

Product number -
Other names N-Benzyl-N-(3-butenyl)-2,2,2-trifluoroacetamide

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:233590-33-5 SDS

233590-33-5Relevant academic research and scientific papers

1,2,3,5-tetrahydrobenzo'c!azepin-4-one derivatives having muscarinic antagonist activity

-

, (2008/06/13)

There is disclosed a compound having the formula or a pharmaceutically acceptable salt thereof, wherein: R1a, R1b and R1c are independently fluorine or hydrogen; R2 is C1 to C12 alkyl being

Synthesis of 2,3-disubstituted pyrrolidines by intramolecular addition of α-aminoalkyl radicals to electron deficient C=C bonds

Aurrecoechea, Jose M.,Fernandez, Alvaro,Gorgojo, Jose M.,Saornil, Carlos

, p. 7345 - 7362 (2007/10/03)

2,3-Disubstituted pyrrolidines are prepared by SmI2-promoted cyclization of α-amino radicals generated from N-(α- benzotriazolylakyl)alkenylamines containing a C=C bond activated by an electron withdrawing substituent. The diastereoselectivity of cyclization is moderate and depends on the nature of the substituent at the pyrrolidine 2- position.

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