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103615-48-1

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103615-48-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103615-48-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,6,1 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 103615-48:
(8*1)+(7*0)+(6*3)+(5*6)+(4*1)+(3*5)+(2*4)+(1*8)=91
91 % 10 = 1
So 103615-48-1 is a valid CAS Registry Number.

103615-48-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(iodoacetyl)tert-butylamine

1.2 Other means of identification

Product number -
Other names N-tert-butyl iodoacetamide

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:103615-48-1 SDS

103615-48-1Relevant articles and documents

Complexes of selected late period lanthanide(III) cations with 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid amide (DOTAM)-alkyl ligands-A new platform for the development of paramagnetic chemical exchange saturation transfer (PARACEST) magnetic resonance imaging (MRI) contrast agents

Elmehriki, Adam A.H.,Milne, Mark,Suchy, Mojmir,Bartha, Robert,Hudson, Robert H.E.

, p. 211 - 219 (2013/05/22)

A series of 18 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid amide (DOTAM)-alkyl derived complexes with selected late lanthanide(III) cations (Dy3+, Tb3+, and Tm3+) has been synthesized; their magnetic properties have been evaluated and compared to those derived from DOTAM. Peralkylation of cyclen with corresponding N-iodoacetyl amines was utilized as the key step in the synthesis. Chemical exchange saturation transfer (CEST) spectra of the complexes have been acquired at 37 C, revealing that Tm3+-derived DOTAM-alkyl complexes possess the most favorable properties as potential paramagnetic chemical exchange saturation transfer (PARACEST) magnetic resonance imaging (MRI) contrast agents.

5-Phenyl-3-ureidobenzazepin-2-ones as cholecystokinin-B receptor antagonists

Lowe III,Hageman,Drozda,McLean,Bryce,Crawford,Zorn,Morrone,Bordner

, p. 3789 - 3811 (2007/10/02)

A series of 5-phenyl-3-ureidobenzazepin-2-one cholecystokinin-B (CCK-B) receptor antagonists was synthesized using Beckmann ring expansion of a suitable 4-phenyl-1-tetralone as a key step. Structure-activity relationship studies revealed the importance of

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