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66444-26-6

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66444-26-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66444-26-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,4,4 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 66444-26:
(7*6)+(6*6)+(5*4)+(4*4)+(3*4)+(2*2)+(1*6)=136
136 % 10 = 6
So 66444-26-6 is a valid CAS Registry Number.

66444-26-6SDS

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 Methyl tert-butyloxycarbonyltyrosyl-(D)alanylglycylphenylalaninate

1.2 Other means of identification

Product number -
Other names Boc-Tyr-D-Ala-Gly-Phe-OMe

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:66444-26-6 SDS

66444-26-6Relevant articles and documents

Biological activity of fragments and analogues of the potent dimeric opioid peptide, biphalin

Lipkowski, Andrzej W.,Misicka, Aleksandra,Davis, Peg,Stropova, Dagmar,Janders, Jacqueline,Lachwa, Magdalena,Porreca, Frank,Yamamura, Henry I.,Hruby, Victor J.

, p. 2763 - 2766 (2007/10/03)

The synthesis and biological activity of two fragments of the very potent opioid peptide biphalin, showed that Tyr-D-Ala-Gly-Phe-NH-NH-Phe is the minimal fragment necessary to express equal affinities and the same biological activity profile as the paren

Synthesis and pharmacological study of some enkephalin analogs in relation to the plurality of opiate receptors

Audigier,Mazarguil,Gout,Cros

, p. 173 - 177 (2007/10/02)

We have synthesized a series of enkephalin analogs and measured their affinity for each type of 'opiate' receptor, the μ receptor and the δ receptor. Furthermore, we have determined their respective antinociceptive activity after intracerebroventricular i

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