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106134-85-4

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106134-85-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106134-85-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,1,3 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 106134-85:
(8*1)+(7*0)+(6*6)+(5*1)+(4*3)+(3*4)+(2*8)+(1*5)=94
94 % 10 = 4
So 106134-85-4 is a valid CAS Registry Number.

106134-85-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (1-(3-chloropropyl)piperidin-4-yl)(phenyl)methanone

1.2 Other means of identification

Product number -
Other names 1-(3-chloropropyl)-4-benzoylpiperidine

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:106134-85-4 SDS

106134-85-4Relevant articles and documents

MENIN-MLL INHIBITORS AND METHODS OF USE THEREOF

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Page/Page column 39 ; 32, (2015/01/09)

The present invention relates generally to compounds that inhibit the binding of menin and MLL or MLL fusion proteins and methods of use thereof. In particular embodiments, the present invention provides compositions comprising piperdine-containing compounds and methods of use thereof to inhibit the interaction of menin with MLL oncoproteins (e.g., MLL1, MLL2, MLL-fusion oncoproteins), for example, for the treatment of leukemia, solid cancers, diabetes, and other diseases dependent on activity of MLL1, MLL2, MLL fusion proteins, MLL-PTD and/or menin.

Tricyclic triazolo derivatives, processes for producing the same and the uses of the same

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, (2008/06/13)

Novel tricyclic triazolo derivatives and pharmaceutically acceptable salts thereof, which are useful as anti-inflammation agents, anti-allergy agents or anti-PAF agents as well as processes for producing the same are disclosed. The triazolo derivatives of

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