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60482-97-5

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60482-97-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60482-97-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,4,8 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 60482-97:
(7*6)+(6*0)+(5*4)+(4*8)+(3*2)+(2*9)+(1*7)=125
125 % 10 = 5
So 60482-97-5 is a valid CAS Registry Number.

60482-97-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-[[(2S,3S)-2-[[(2S)-3-(4-hydroxyphenyl)-2-[[(2S)-pyrrolidine-2-carbonyl]amino]propanoyl]amino]-3-methylpentanoyl]amino]-4-methylpentanoic acid

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:60482-97-5 SDS

60482-97-5Downstream Products

60482-97-5Relevant articles and documents

Synthesis of Peptides by the Solid-Phase Method. 6. Neurotensin, Fragments, and Analogues

St-Pierre, S.,Lalonde, J.-M.,Gendreau, M.,Quirion, R.,Regoli, D.,Rioux, F.

, p. 370 - 376 (2007/10/02)

Neurotensin (NT) and 24 related compounds, including fragments or analogues modified at the C-terminal end of the parent molecule, have been prepared by the solid-phase method.After purification by cation-exchange chromatography, the compounds were characterized by thin-layer chromatography, amino acid analysis, elemental analysis, and high-pressure liquid chromatography.The stimulating effects of the peptides were evaluated in rat stomach strips, in isolated spontaneously beating atria of guinea pigs, and in the coronaries of perfused rat hearts.The differences between the biological activities of these compounds are discussed.

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