CAS 6404-29-1

6-[(tert-Butoxycarbonyl)amino]hexanoic acid

Description:

6-[(tert-Butoxycarbonyl)amino]hexanoic acid, with the CAS number 6404-29-1, is an amino acid derivative characterized by the presence of a hexanoic acid backbone and a tert-butoxycarbonyl (Boc) protecting group on the amino functional group. This compound typically appears as a white to off-white solid and is soluble in organic solvents such as dichloromethane and dimethyl sulfoxide, but has limited solubility in water. The Boc group serves as a protective moiety, making the compound useful in peptide synthesis and other organic reactions, as it can be easily removed under acidic conditions. The presence of both the carboxylic acid and amine functional groups allows for the formation of peptide bonds, facilitating its role in the synthesis of more complex molecules. Additionally, the compound's structure contributes to its potential applications in pharmaceuticals and biochemistry, particularly in the development of peptide-based drugs. Proper handling and storage are essential, as with many chemical substances, to ensure safety and stability.

Formula: C₁₁H₂₁NO₄

InChI: InChI=1S/C11H21NO4/c1-11(2,3)16-10(15)12-8-6-4-5-7-9(13)14/h4-8H2,1-3H3,(H,12,15)(H,13,14)

InChI key: InChIKey=RUFDYIJGNPVTAY-UHFFFAOYSA-N

SMILES: O(C(NCCCCCC(O)=O)=O)C(C)(C)C

Synonyms:

• 1-tert-Butoxycarbonylamino-6-hexanoic acid
• 6-(tert-Butoxycarbonylamino)caproic acid
• 6-[(Tert-Butoxycarbonyl)Amino]Hexanoic Acid
• 6-[N-(tert-Butoxycarbonyl)amino]caproic acid
• 6-[[(1,1-Dimethylethoxy)carbonyl]amino]hexanoic acid
• BOC-ε-aminocaproic acid
• Boc-6-Ahx-OH
• Boc-6-aminocaproic acid
• Boc-6-aminohexanoic acid
• Boc-EAhx-OH
• Boc-e-Acp-OH
• Hexanoic acid, 6-(carboxyamino)-, 6-tert-butyl ester
• Hexanoic acid, 6-(carboxyamino)-, N-tert-butyl ester
• Hexanoic acid, 6-[[(1,1-dimethylethoxy)carbonyl]amino]-
• N-(tert-Butoxycarbonyl)-6-aminocaproic acid
• N-(tert-Butoxycarbonyl)-6-aminohexanoic acid
• N-(tert-Butoxycarbonyl)-ε-aminocaproic acid
• N-(tert-Butoxycarbonyl)-ε-aminohexanoic acid
• N-(tert-Butyloxycarbonyl)-ε-aminocaproic acid
• N-BOC-6-aminocaproic acid
• N-Boc-aminohexanoic acid
• N-T-boc-6-aminohexanoic acid

N-(tert-Butoxycarbonyl)-6-aminohexanoic Acid

CAS: 6404-29-1

Formula: C₁₁H₂₁NO₄

Purity: >95.0%(GC)(T)

Color and Shape: White to Light yellow powder to lump

Molecular weight: 231.29

Ref: 3B-B4275

6-(Boc-amino)hexanoic acid, 95%

CAS: 6404-29-1

6-(Boc-amino)hexanoic acid is used in the preparation of esters of 6-aminohexanoic acid as antibacterial agents. EACA is reported to inhibit chymotrypsin, Factor VIIa, lysine carboxy peptidase, plasmin, and plasminogen activator. This Thermo Scientific Chemicals brand product was originally part of

Formula: C₁₁H₂₁NO₄

Purity: 95%

Molecular weight: 231.29

Ref: 02-H61350

Boc-ε-aminocaproic acid

CAS: 6404-29-1

Also called Boc-LC.

Formula: C₁₁H₂₁NO₄

Purity: > 99%

Color and Shape: White

Molecular weight: 231.29

Ref: 01-4000005

Boc-ε-Acp-OH

CAS: 6404-29-1

Formula: C₁₁H₂₁NO₄

Purity: 97%

Color and Shape: Solid

Molecular weight: 231.2887

Ref: IN-DA003OFM

Boc-εAhx-OH

CAS: 6404-29-1

Boc-εAhx-OH

Purity: 98%

Molecular weight: 231.29g/mol

Ref: 54-OR36348

Boc-6-Ahx-OH

CAS: 6404-29-1

Formula: C₁₁H₂₁NO₄

Purity: ≥ 98.0%

Color and Shape: White to off-white powder

Molecular weight: 231.29

Ref: 7W-GM3318

Boc-6-aminohexanoic acid

CAS: 6404-29-1

Boc-6-aminohexanoic acid is an alkyl/ether-based linker employed in PROTAC synthesis.

Formula: C₁₁H₂₁NO₄

Color and Shape: Solid

Molecular weight: 231.29

Ref: TM-T40737

Boc-6-aminohexanoic acid

CAS: 6404-29-1

Boc-6-aminohexanoic acid is a macrocyclization compound that has been shown to be an effective adjuvant for vaccines. It is also a potent immune stimulator and has the potential to be used in the development of new types of devices and drugs. Boc-6-aminohexanoic acid is a synthetic compound that was created using advances in organic chemistry, with properties similar to those found in natural products. This compound can be used as an adjuvant for vaccines, and has been shown to have immune reactivity similar to saponins, which are natural products.

Formula: C₁₁H₂₁NO₄

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 231.29 g/mol

Ref: 3D-FB33656

boc-E-acp-oh

CAS: 6404-29-1

Formula: C₁₁H₂₁NO₄

Purity: 97%

Color and Shape: Solid

Molecular weight: 231.292

Ref: 10-F045379

tert-Butoxycarbonyl-ε-aminocaproic Acid

Controlled Product

CAS: 6404-29-1

Applications Protected ε-Aminocaproic Acid (A603015). Used in the preparatiom of esters of 6-aminohexanoic acid as antibacterial agents. EACA is reported to inhibit chymotrypsin, Factor VIIa, lysine carboxy peptidase, plasmin, and plasminogen activator.
References Dolezal, P., et al.: Pharm. Res., 10, 1015 (1993), Vavrova, K., et al.: Curr. Med. Chem., 12, 2273 (2005), Holas, T., et al.: Bioorg. Med. Chem., 14, 7671 (2006),

Formula: C₁₁H₂₁NO₄

Color and Shape: Neat

Molecular weight: 231.29

Ref: TR-B690655