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4-(ChloroMethyl)-N-cyclopropylbenzaMide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

873371-67-6

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873371-67-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 873371-67-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,3,3,7 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 873371-67:
(8*8)+(7*7)+(6*3)+(5*3)+(4*7)+(3*1)+(2*6)+(1*7)=196
196 % 10 = 6
So 873371-67-6 is a valid CAS Registry Number.

873371-67-6SDS

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 4-chloromethyl-N-cyclopropyl-banzamide

1.2 Other means of identification

Product number -
Other names 4-chloromethyl-N-cyclopropyl-benzamide

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:873371-67-6 SDS

873371-67-6Downstream Products

873371-67-6Relevant academic research and scientific papers

Synthesis and biological evaluation of 2,4-disubstituted phthalazinones as Aurora kinase inhibitors

Wang, Wei,Feng, Xiu,Liu, Huan-Xiang,Chen, Shi-Wu,Hui, Ling

, p. 3217 - 3226 (2018)

A series of 2,4-disubstituted phthalazinones were synthesized and their biological activities, including antiproliferation, inhibition against Aurora kinases and cell cycle effects were evaluated. Among them, N-cyclohexyl-4-((4-(1-methyl-1H-pyrazol-4-yl)-1-oxophthalazin-2(1H)-yl) methyl) benzamide (12c) exhibited the most potent antiproliferation against five carcinoma cell lines (HeLa, A549, HepG2, LoVo and HCT116 cells) with IC50 values in range of 2.2–4.6 μM, while the IC50 value of reference compound VX-680 was 8.5–15.3 μM. Moreover, Aurora kinase assays exhibited that compound 12c was potent inhibitor of AurA and AurB kinase with the IC50 values were 118 ± 8.1 and 80 ± 4.2 nM, respectively. Molecular docking studies indicated that compound 12c forms better interaction with both AurA and AurB. Furthermore, compound 12c induced G2/M cell cycle arrest in HeLa cells by regulating protein levels of cyclinB1 and cdc2. These results suggested that 12c is a promising pan-Aurora kinase inhibitor for the potential treatment of cancer.

Sulfonamides

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Page/Page column 50, (2010/02/15)

The invention relates to compounds of the general formula in which R1, R2, R3, R4, R2′, R3′, R4′, R5, and X is —CHR— are as defined in the specification. The invention also provides pharmac

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