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1003028-41-8

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1003028-41-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1003028-41-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,3,0,2 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1003028-41:
(9*1)+(8*0)+(7*0)+(6*3)+(5*0)+(4*2)+(3*8)+(2*4)+(1*1)=68
68 % 10 = 8
So 1003028-41-8 is a valid CAS Registry Number.

1003028-41-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(3-morpholin-4-yl-propoxy)phenylboronic acid

1.2 Other means of identification

Product number -
Other names (3-(3-morpholinopropoxy)phenyl)boronic acid

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:1003028-41-8 SDS

1003028-41-8Upstream product

1003028-41-8Downstream Products

1003028-41-8Relevant articles and documents

Synthesis and preliminary evaluation of novel analogues of quindolines as potential stabilisers of telomeric G-quadruplex DNA

Le Sann, Christine,Huddleston, Jonathan,Mann, John

, p. 12903 - 12911 (2007)

Telomeric DNA is a potential selective target for cancer therapy since the tumour-associated enzyme telomerase regulates telomere maintenance in most cancer cells. The 3′ single-stranded ends of telomeric DNA can be folded into quadruplex structures by appropriate small molecules. We describe the preparation of a new class of 2,7-disubstituted 10H-indolo[3,2-b]quinolines with enhanced selectivity for the stabilisation of quadruplex DNA compared to duplex DNA, and also the preparation of a key intermediate for the synthesis of trisubstituted quindolines.

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