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500770-68-3

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500770-68-3 Usage

General Description

BOC-(S)-3-AMINO-3-(1-NAPHTHYL)-PROPIONIC ACID is a chemical compound with the molecular formula C21H23NO4. It is a derivative of 3-amino-3-(1-naphthyl)propionic acid and contains a BOC (tert-butyloxycarbonyl) protecting group. The compound is commonly used in organic synthesis and pharmaceutical research as a building block for the synthesis of various amino acids and peptides. It is a chiral compound, meaning it has a specific spatial arrangement of its atoms, with the (S)-enantiomer being the active form. BOC-(S)-3-AMINO-3-(1-NAPHTHYL)-PROPIONIC ACID is typically handled and stored according to standard laboratory procedures for chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 500770-68-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,0,7,7 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 500770-68:
(8*5)+(7*0)+(6*0)+(5*7)+(4*7)+(3*0)+(2*6)+(1*8)=123
123 % 10 = 3
So 500770-68-3 is a valid CAS Registry Number.

500770-68-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S)-3-[(2-methylpropan-2-yl)oxycarbonylamino]-3-naphthalen-1-ylpropanoic acid

1.2 Other means of identification

Product number -
Other names BOC-D-GLY(1-NAPH)-(C*CH2)OH

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:500770-68-3 SDS

500770-68-3Upstream product

500770-68-3Downstream Products

500770-68-3Relevant articles and documents

Synthesis and biological activity of somatostatin analogs modified at the tryptophan residue.

Yabe et al.

, p. 993,996 (2007/10/09)

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