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1217603-41-2

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1217603-41-2 Usage

General Description

FMoc-(S)-2-amino-3-hydroxy-3-methylbutanoic acid is a chemical compound used in the synthesis of peptides and proteins. It is a derivative of the natural amino acid threonine, with an added FMoc (9-fluorenylmethoxycarbonyl) protective group for the amino group. FMoc-(S)-2-aMino-3-hydroxy-3-Methylbutanoic acid is commonly used in solid-phase peptide synthesis due to its stability and ability to selectively protect the hydroxyl and amino groups during the synthesis process. It is also used in the development of pharmaceuticals, as well as in biochemical and biotechnological research. Overall, FMoc-(S)-2-amino-3-hydroxy-3-methylbutanoic acid plays a crucial role in the production of complex peptides and proteins for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1217603-41-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,7,6,0 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1217603-41:
(9*1)+(8*2)+(7*1)+(6*7)+(5*6)+(4*0)+(3*3)+(2*4)+(1*1)=122
122 % 10 = 2
So 1217603-41-2 is a valid CAS Registry Number.

1217603-41-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Fmoc-L-Val(β-OH)-OH

1.2 Other means of identification

Product number -
Other names Fmoc-(S)-2-amino-3-hydroxy-3-methylbutanoic acid

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:1217603-41-2 SDS

1217603-41-2Downstream Products

1217603-41-2Relevant articles and documents

Gold-Catalyzed Amide/Carbamate-Linked N, O-Acetal Formation with Bulky Amides and Alcohols

Ohsawa, Kosuke,Ochiai, Shota,Kubota, Junya,Doi, Takayuki

, p. 1281 - 1291 (2021/01/14)

A gold-catalyzed N,O-acetal formation was established to construct an amide/carbamate-linked N,O-acetal substructure with bulky alcohols. The acyliminium cation species generated from o-alkynylbenzoic acid ester in the presence of a gold catalyst is highly reactive and underwent nucleophilic attack of various bulky alcohols and phenols at room temperature under neutral conditions, leading to the corresponding N,O-acetals in yields of 34-89% with good functional group tolerance.

COMPOUNDS FOR THE TREATMENT OF BOVINE OR SWINE RESPIRATORY DISEASE

-

Page/Page column 162, (2018/07/29)

The present invention provides compounds for use in the treatment of respiratory diseases of animals, especially Bovine or Swine Respiratory disease (BRD and SRD).

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