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1,4,7,10-Tetraazacyclododecane-1,4-diacetic acid, bis(1,1-dimethylethyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

507475-91-4

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507475-91-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 507475-91-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,7,4,7 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 507475-91:
(8*5)+(7*0)+(6*7)+(5*4)+(4*7)+(3*5)+(2*9)+(1*1)=164
164 % 10 = 4
So 507475-91-4 is a valid CAS Registry Number.

507475-91-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name di-tert-butyl 2,2'-(1,4,7,10-tetraazacyclododecane-1,4-diyl)diacetate

1.2 Other means of identification

Product number -
Other names -

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:507475-91-4 SDS

507475-91-4Downstream Products

507475-91-4Relevant academic research and scientific papers

A selective one-step synthesis of tris N-alkylated cyclens

Li, Cong,Wong, Wing-Tak

, p. 5595 - 5601 (2004)

A general one-step synthesis for tris N-alkylated cyclens with good yield and unprecedented selectivity is presented. Tris and 1,4-bis N-alkylated cyclens, as the only two major products are isolated. Furthermore, according to the single crystal X-ray str

SYNTHESIS OF TRIS N-ALKYLATED 1,4,7,10-TETRAAZACYCLODODECANES

-

Page/Page column 6, (2008/06/13)

A directly synthetic method for preparing tris-alkylated 1,4,7,10-tetraazacyclododecanes by the reactions of 1,4,7,10-tetraazacyclododecane (cyclen) and appropriate electrophiles is accomplished in high yield. The method provides operational convenience,

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