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98628-27-4

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98628-27-4 Usage

General Description

Boc-L-2-Amino-5-phenyl-pentanoic acid is a chemical compound with the molecular formula C18H25NO4. It is classified as a peptide, containing a protecting group named Boc (tert-butyloxycarbonyl) attached to the N-terminal of the amino acid L-2-Amino-5-phenyl-pentanoic acid. Boc-L-2-Amino-5-phenyl-pentanoic acid is commonly used in the synthesis of peptides and pharmaceuticals due to its ability to protect the amino acid residues during chemical reactions. It is also used as a building block for the preparation of complex organic molecules. Its unique structure and properties make it an important reagent in organic and medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 98628-27-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,6,2 and 8 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 98628-27:
(7*9)+(6*8)+(5*6)+(4*2)+(3*8)+(2*2)+(1*7)=184
184 % 10 = 4
So 98628-27-4 is a valid CAS Registry Number.

98628-27-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-2-((tert-Butoxycarbonyl)amino)-5-phenylpentanoic acid

1.2 Other means of identification

Product number -
Other names (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-5-phenylpentanoic 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:98628-27-4 SDS

98628-27-4Relevant articles and documents

Organocatalytic one-pot oxidative cleavage of terminal diols to dehomologated carboxylic acids

Shibuya, Masatoshi,Doi, Ryusuke,Shibuta, Takuro,Uesugi, Shun-Ichiro,Iwabuchi, Yoshiharu

, p. 5006 - 5009 (2013/01/15)

The organocatalytic one-pot oxidative cleavage of terminal 1,2-diols to one-carbon-unit-shorter carboxylic acids is described. The combination of 1-Me-AZADO (cat.), NaOCl (cat.), and NaClO2 caused smooth one-pot oxidative cleavage under mild conditions. A broad range of substrates including carbohydrates and N-protected amino diols were converted without epimerization. Terminal triols and tetraols respectively underwent cleavage of their C-2 and C-3 moieties to afford their corresponding two- and three-carbon-unit-shorter carboxylic acids.

Solid-phase synthesis of dehydropeptide, AM-toxin II, using a novel selenyl linker by side-chain tethered strategy

Horikawa, Eiji,Kodaka, Masato,Nakahara, Yoshiaki,Okuno, Hiroaki,Nakamura, Kazuhiko

, p. 8337 - 8339 (2007/10/03)

The cyclic dehydrodepsipeptide, AM-toxin II, was efficiently synthesized by a solid-phase method using a novel selenyl linker. The cleavage from the resin with formation of a double bond is successfully achieved under mild oxidative conditions with TBHP.

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