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228245-16-7

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228245-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 228245-16-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,8,2,4 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 228245-16:
(8*2)+(7*2)+(6*8)+(5*2)+(4*4)+(3*5)+(2*1)+(1*6)=127
127 % 10 = 7
So 228245-16-7 is a valid CAS Registry Number.

228245-16-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(N-Boc-aminooxy)propylamine

1.2 Other means of identification

Product number -
Other names tert-butyl 3-aminopropoxycarbamate

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:228245-16-7 SDS

228245-16-7Downstream Products

228245-16-7Relevant articles and documents

Peptide microarrays for the determination of protease substrate specificity

Salisbury, Cleo M.,Maly, Dustin J.,Ellman, Jonathan A.

, p. 14868 - 14870 (2002)

A method is described for the preparation of substrate microarrays that allow for the rapid determination of protease substrate specificity. Peptidyl coumarin substrates, synthesized on solid support using standard techniques, are printed onto glass slide

FLUORESCENT PROBES FOR ABASIC SITE DETECTION

-

, (2016/11/02)

A fluorescent probe for binding to and detection of AP sites of DNA includes the following formula: F-L-X where F is a fluorescent moiety, X is an aminooxy group (-ONH2), and L is a linker that links or couples the fluorescent moiety to the oxy

Designer macrocyclic organo-peptide hybrids inhibit the interaction between p53 and HDM2/X by accommodating a functional α-helix

Smith, Jessica M.,Frost, John R.,Fasan, Rudi

supporting information, p. 5027 - 5030 (2014/05/06)

We report the design of side-chain-to-tail linked organo-peptide hybrids incorporating an α-helical protein-binding motif. Using this strategy, macrocyclic inhibitors of the p53:HDM2 interaction displaying dual specificity against the HDMX homolog as well

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