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67230-47-1

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67230-47-1 Usage

General Description

BOC-Phe(3,5-DII,4-NH2)-OH is a chemical compound that is used in the field of organic chemistry. It is a derivative of the amino acid phenylalanine, and it contains a BOC (tert-butoxycarbonyl) protecting group, as well as additional functional groups at specific positions on the phenyl ring. BOC-PHE(3,5-DII,4-NH2)-OH is commonly used as a building block in peptide synthesis, where it serves as a starting material for the production of custom-designed peptides with specific sequences. The BOC protecting group is important for preventing unwanted chemical reactions during the synthesis process, while the additional functional groups can be used to tailor the properties of the resulting peptides for specific applications. Overall, BOC-Phe(3,5-DII,4-NH2)-OH plays a crucial role in the production of customized peptides for various research and therapeutic purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 67230-47-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,2,3 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 67230-47:
(7*6)+(6*7)+(5*2)+(4*3)+(3*0)+(2*4)+(1*7)=121
121 % 10 = 1
So 67230-47-1 is a valid CAS Registry Number.

67230-47-1SDS

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 BOC-PHE(3,5-DII,4-NH2)-OH

1.2 Other means of identification

Product number -
Other names BOC-PHE(4-NH2-3,5-I2)-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:67230-47-1 SDS

67230-47-1Upstream product

67230-47-1Downstream Products

67230-47-1Relevant articles and documents

Photoaffinity labeling of the angiotensin II receptor. 1. Synthesis and biological activities of the labeling peptides.

Escher et al.

, p. 860,862 (1978)

The synthesis and biological activities of analogues of the peptide hormone angiotensin II (AT) for use in photoaffinity labeling and receptor isolation are described. In the modified sequence of AT, Sar-Arg-Val-Tyr-Val-His-Pro-Phe, the aromatic residues

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