ALPHA-BOC-GAMMA-Z-(DL)-DIAMINOBUTYRIC ACID

ALPHA-BOC-GAMMA-Z-(DL)-DIAMINOBUTYRIC ACID - Names and Identifiers

Name	Boc-Dab(Z)-OH . DCHA
Synonyms	BOC-DAB(Z)-OH DCHA Boc-Dab(Z)-OH·DCHA Boc-Dab(Z)-OH . DCHA BOC-L-DAB(Z)-OH DCHA N-cyclohexylcyclohexanamine Alpha-Boc-Gamma-Z-(Dl)-Diaminobutyric Acid ALPHA-BOC-GAMMA-Z-(DL)-DIAMINOBUTYRIC ACID BOC-ALPHA,GAMMA-DIAMINOBUTYRIC ACID(Z)-OH DCHA (2S)-2-(tert-butoxycarbonylamino)-4-(carboxyamino)butanoic acid BOC-N-GAMMA-Z-L-2,4-DIAMINOBUTYRIC ACID DICYCLOHEXYLAMMONIUM SALT N-alpha-Boc-Ngamma-Z-L-2,4-diaminobutyric acid dicyclohexylammonium salt (2S)-4-{[(benzyloxy)carbonyl]amino}-2-{[(tert-butoxy)carbonyl]amino}butanoic acid (S)-2-[[(1,1-DIMETHYLETHOXY)CARBONYL]AMINO]-4-[[(PHENYLMETHOXY)CARBONYL]AMINO] BUTANOIC ACID, DICYCLOHEXYLAMINE SALT
CAS	16947-89-0
InChI	InChI=1/C12H23N.C10H18N2O6.C8H10/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12;1-10(2,3)18-9(17)12-6(7(13)14)4-5-11-8(15)16;1-2-8-6-4-3-5-7-8/h11-13H,1-10H2;6,11H,4-5H2,1-3H3,(H,12,17)(H,13,14)(H,15,16);3-7H,2H2,1H3/t;6-;/m.0./s1

ALPHA-BOC-GAMMA-Z-(DL)-DIAMINOBUTYRIC ACID - Physico-chemical Properties

Molecular Formula	C17H24N2O6
Molar Mass	352.38
Boling Point	719.6°C at 760 mmHg
Flash Point	389°C
Vapor Presure	9.85E-22mmHg at 25°C
Storage Condition	Inert atmosphere,2-8°C

ALPHA-BOC-GAMMA-Z-(DL)-DIAMINOBUTYRIC ACID - Introduction

Boc-Dab(Z)-OH . DCHA is a drug molecule, usually abbreviated as CBDA, with the chemical structure N-(tert-butoxycarbonyl)-N'-benzyloxycarbonyl-L-2,4-diaminobutanoic acid dihexylamine salt.

CBDA is a white solid with good stability at room temperature. It is soluble in commonly used solvents such as ethanol and dimethyl sulfoxide.

CBDA has many uses. As an intermediate in the field of pharmaceutical research, it is commonly used in the synthesis of polypeptide drugs and analogs of natural products. In addition, CBDA can also be used as a protein cross-linking reagent and ribonucleic acid (DNA/RNA) cross-linking reagent.

The preparation method of CBDA generally includes the following steps: First, L-2, 4-diaminobutyric acid is reacted with tert-butyryl chloride to obtain N-tert-butoxycarbonyl-L-2,4-diaminobutyric acid; Then, the obtained product is reacted with benzyl alcohol to generate N-tert-butoxycarbonyl-N'-benzyloxycarbonyl-L-2, 4-diaminobutyric acid; Finally, this molecule is reacted with cyclohexylamine to form the dicyclohexylamine salt.

The safety information of CBDA is not particularly clear. Because it is a pharmaceutical intermediate, appropriate chemical laboratory safety measures should be taken during handling and handling, such as wearing personal protective equipment, maintaining good ventilation, and avoiding inhalation or contact with skin and eyes. If you have accidentally ingested or come into contact with CBDA, you should seek medical help immediately and bring along the product label or container for reference.

Last Update：2024-04-09 21:01:54