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Butanediamide, 2-amino-, (2S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16748-73-5

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16748-73-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16748-73-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,4 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16748-73:
(7*1)+(6*6)+(5*7)+(4*4)+(3*8)+(2*7)+(1*3)=135
135 % 10 = 5
So 16748-73-5 is a valid CAS Registry Number.

16748-73-5SDS

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 (2S)-2-aminobutanediamide

1.2 Other means of identification

Product number -
Other names L-aspartic acid diamide

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:16748-73-5 SDS

16748-73-5Relevant academic research and scientific papers

Polyaspartamide derivatives as adsorbents for bile acids, polyaspartamide derivatives loaded with bile acids and process for their preparation and their use as pharmaceuticals

-

, (2008/06/13)

Polyaspartamide derivatives as adsorbents for bile acids, polyaspartamide derivatives loaded with bile acids and process for their preparation and their use as pharmaceuticals α- or β-linked polyaspartamide derivatives of the formula I STR1 in which RI RII, RIII, RIV, r, s, t, u and v have the stated meanings, are described. They adsorb bile acids and can be used as pharmaceuticals.

SYNTHESIS OF PYROGLUTAMYLASPARAGINE AMIDE DIPEPTIDE FRAGMENT OF VASOPRESSIN, AND THE STEREOSELECTIVITY OF ITS MNEMIC EFFECT

Gudasheva, T. A.,Rozantsev, G. G.,Ostrovskaya, R. U.,Trofimov, S. S.,Voronina, T. A.,et al.

, p. 14 - 17 (2007/10/03)

Four diastereomers of pGlu-Asn-NH2 were synthesized.They were considered on one hand as a peptide analogue of piracetam, and on the other as an N-terminal fragment of the major metabolite of vasopressin 4, Cyt6>AVP(4-9).The influence of these diastereomers on the memory of rats was studied in the passive avoidance conditioned reflex test.It was shown that L-pGlu-L-Asn-NH2 and D-pGlu-D-Asn-NH2 in the same doses facilitate the training of rats; D-pGlu-D-Asn-NH2 is inactive, and L-pGlu-D-Asn-NH2 has amnestic activity.These facts suggest a receptor mechanism for the action of the dipeptide pGlu-Asn-NH2 and are the basis for a hypothesis for the topology of the nootropic receptor binding site.

Peptide Synthesis in Alcohol Solvents by the Mixed Anhydride Method Using Dimethylphosphinothioyl Chloride

Ueki, Masaaki,Saito, Takashi,Sasaya, Jun,Ikeda, Shigeru,Oyamada, Hidekazu

, p. 3653 - 3658 (2007/10/02)

The formation and coupling of the dimethylphosphinothioic mixed anhydrides of protected amino acids can be performed in alcohol solvents.Sparingly soluble protected C-terminal segments of vasoactive intestinal peptide (VIP) up to the heptapeptide stage we

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