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14037-86-6

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14037-86-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14037-86-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,3 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 14037-86:
(7*1)+(6*4)+(5*0)+(4*3)+(3*7)+(2*8)+(1*6)=86
86 % 10 = 6
So 14037-86-6 is a valid CAS Registry Number.

14037-86-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-bromopropyl 3,4,5-trimethoxybenzoate

1.2 Other means of identification

Product number -
Other names 3,4,5-trimethoxy-benzoic acid-(3-bromo-propyl ester)

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:14037-86-6 SDS

14037-86-6Relevant articles and documents

Gallic acid acylated derivatives having anticancer activity and use thereof

-

, (2017/08/28)

The invention discloses gallic acid acylated derivatives having anticancer activity. The gallic acid acylated derivatives have a structural formula shown in the description. The acylated derivatives provided by the invention have good activity to oral cancer cells, have good selectivity and have a good clinical application value.

Dilazep analogues for the study of equilibrative nucleoside transporters 1 and 2 (ENT1 and ENT2)

Playa, Hilaire,Lewis, Timothy A.,Ting, Amal,Suh, Byung-Chul,Muoz, Benito,Matuza, Robert,Passer, Brent J.,Schreiber, Stuart L.,Buolamwini, John K.

supporting information, p. 5801 - 5804 (2015/01/08)

As ENT inhibitors including dilazep have shown efficacy improving oHSV1 targeted oncolytic cancer therapy, a series of dilazep analogues was synthesized and biologically evaluated to examine both ENT1 and ENT2 inhibition. The central diamine core, alkyl chains, ester linkage and substituents on the phenyl ring were all varied. Compounds were screened against ENT1 and ENT2 using a radio-ligand cell-based assay. Dilazep and analogues with minor structural changes are potent and selective ENT1 inhibitors. No selective ENT2 inhibitors were found, although some analogues were more potent against ENT2 than the parent dilazep.

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