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7160-44-3

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7160-44-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7160-44-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,6 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7160-44:
(6*7)+(5*1)+(4*6)+(3*0)+(2*4)+(1*4)=83
83 % 10 = 3
So 7160-44-3 is a valid CAS Registry Number.

7160-44-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-oxa-3-azabicyclo[2.2.2]oct-5-ene

1.2 Other means of identification

Product number -
Other names 2-oxa-3-aza-bicyclo[2.2.2]oct-5-ene

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:7160-44-3 SDS

7160-44-3Relevant articles and documents

NOVEL BINDER-DRUG CONJUGATES (ADCs) AND USE OF SAME

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Paragraph 3728-3730, (2015/10/05)

The present patent application relates to novel binder-drug conjugates (ADCs) of N,N-dialkylauristatins directed against the target epidermal growth factor receptor (EGFR, gene ID 1956), effective metabolites of these ADCs, methods for producing these ADCs, use of these ADCs for treatment and or prevention of diseases as well as the use of these ADCs to produce pharmaceutical drugs for treatment and/or prevention of diseases, in particular hyperproliferative and/or angiogenic diseases such as cancer, for example. Such treatments may be administered as monotherapy or in combination with other pharmaceutical drugs or other therapeutic measures.

Auristatin derivatives and use thereof

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Page/Page column, (2014/05/20)

The present application relates to novel derivatives of monomethylauristatin F, to processes for preparing these derivatives, to the use of these derivatives for treating and/or preventing diseases, and also to the use of these derivatives for preparing medicaments for treating and/or preventing diseases, more particularly hyperproliferative and/or angiogenic disorders such as, for example, cancerous disorders. Such treatments may be practised as a monotherapy or else in combination with other medicaments or further therapeutic measures.

Syntheses of conformationally constricted molecules as potential NAALADase/PSMA inhibitors

Ding, Pingyu,Miller, Marvin J.,Chen, Yi,Helquist, Paul,Oliver, A. Jayne,Wiest, Olaf

, p. 1805 - 1808 (2007/10/03)

Matrix presented. Two six-membered ring targeted analogues of PSMA inhibitors (4a and 4b) were designed on the basis of a computational analysis and synthesized. (E,Z)-Diene 10 was subjected to the nitroso Diels-Alder reaction to give the 1,4-trans six-me

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