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4-Amino-2-[(1,1-dimethylethoxy)carbonyl]amino]butanoic acid is a complex organic compound with the molecular formula C9H18N2O4. It is a derivative of amino acids, featuring an amino group at the 4-position and a protected amino group at the 2-position, which is attached to a 1,1-dimethylethoxycarbonyl (tert-butoxycarbonyl or Boc) group. 4-Amino-2- [ (1,1-dimethylethoxy)carbonyl]amino]butanoic acid is significant in organic synthesis and pharmaceutical chemistry, particularly for the protection of amino groups during peptide synthesis. The Boc group can be removed under acidic conditions, which is crucial for the selective deprotection of amino groups in the synthesis of complex peptides and proteins. Its unique structure and reactivity make it a valuable intermediate in the preparation of various bioactive molecules and pharmaceuticals.

2899-79-8

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2899-79-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2899-79-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,9 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2899-79:
(6*2)+(5*8)+(4*9)+(3*9)+(2*7)+(1*9)=138
138 % 10 = 8
So 2899-79-8 is a valid CAS Registry Number.

2899-79-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name L-Boc-Dab-OH

1.2 Other means of identification

Product number -
Other names Boc-Dab-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:2899-79-8 SDS

2899-79-8Upstream product

2899-79-8Downstream Products

2899-79-8Relevant academic research and scientific papers

Synthesis method of 2,4-diaminobutyric acid derivative

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Paragraph 0086-0089, (2021/03/11)

The invention belongs to the field of organic chemistry, and particularly relates to a synthesis method of a 2,4-diaminobutyric acid derivative. According to the synthesis method of the 2,4-diaminobutyric acid and the derivative thereof provided by the invention, homoserine is selected as an initial raw material, the amino and carboxyl of the homoserine are protected firstly, a pht group is introduced through a light delay reaction, and then a final product can be obtained through six steps of benzyl ester removal, pht removal and Boc group removal. According to the invention, the synthetic method provided by the invention has relatively high reaction yield and is convenient for separation and purification; the intermediates obtained in the reaction are all protecting group modified aminoacid derivatives and can be directly used as drug intermediates or raw materials for synthesizing other compounds, so that waste is avoided; and the reaction conditions provided by the invention are mild, and later-period amplification production is facilitated.

Aminoethylglycine containing polypeptides

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, (2008/06/13)

Novel somatostatin analogues containing one or more aminoethylglycyl residues at the amino and/or carboxyl terminus or in the ring position are described. The compounds are potent and long lasting inhibitors of gastric acid secretion.

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