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N-(1,3-benzodioxol-5-ylmethyl)-2,2,2-trifluoro-N-(2-(4-hydroxyphenyl)ethyl)acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40135-88-4

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40135-88-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40135-88-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,1,3 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 40135-88:
(7*4)+(6*0)+(5*1)+(4*3)+(3*5)+(2*8)+(1*8)=84
84 % 10 = 4
So 40135-88-4 is a valid CAS Registry Number.

40135-88-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(1,3-benzodioxol-5-ylmethyl)-2,2,2-trifluoro-N-[2-(4-hydroxyphenyl)ethyl]acetamide

1.2 Other means of identification

Product number -
Other names -

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:40135-88-4 SDS

40135-88-4Downstream Products

40135-88-4Relevant academic research and scientific papers

METHODS FOR TREATMENT OF RESISTANT CANCER

-

, (2017/11/16)

The present disclosure describes a method to treat conditions, including cancer, using compounds that can target resistant cancer cells. The compounds of the invention can decrease the rate of proliferation of drug-resistant cancer cells, such as glioma,

5,10b-Ethanophenanthridine amaryllidaceae alkaloids inspire the discovery of novel bicyclic ring systems with activity against drug resistant cancer cells

Henry, Sean,Kidner, Ria,Reisenauer, Mary R.,Magedov, Igor V.,Kiss, Robert,Mathieu, Véronique,Lefranc, Florence,Dasari, Ramesh,Evidente, Antonio,Yu, Xiaojie,Ma, Xiuye,Pertsemlidis, Alexander,Cencic, Regina,Pelletier, Jerry,Cavazos, David A.,Brenner, Andrew J.,Aksenov, Alexander V.,Rogelj, Snezna,Kornienko, Alexander,Frolova, Liliya V.

, p. 313 - 328 (2016/06/01)

Plants of the Amaryllidaceae family produce a large variety of alkaloids and non-basic secondary metabolites, many of which are investigated for their promising anticancer activities. Of these, crinine-type alkaloids based on the 5,10b-ethanophenanthridin

Synthesis of Amaryllidaceae alkaloids, siculine, oxocrinine, epicrinine, and buflavine

Kodama, Sumiaki,Takita, Hirofumi,Kajimoto, Tetsuya,Nishide, Kiyoharu,Node, Manabu

, p. 4901 - 4907 (2007/10/03)

Three crinane type of alkaloids isolated from Amaryllidaceae family were synthesized by taking advantage of the PIFA-mediated intramolecular p-p′ diphenol coupling reaction of norbelladine derivatives. Furthermore, buflavine was also prepared by using the p-p′ diphenol coupling followed by dienone-phenol rearrangement as a key step.

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