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BOC-7-AMINO-HEPTANOIC ACID

Product Name
BOC-7-AMINO-HEPTANOIC ACID
CAS No.
60142-89-4
Chemical Name
BOC-7-AMINO-HEPTANOIC ACID
Synonyms
BOC-7-AHP-OH;BOC-AHEPT-OH;BOC-NH-(CH2)6-COOH;Boc-7-aminoheptanoicaci;BOC-7-AMINO-HEPTANOIC ACID;7-(BOC-AMINO)ENANTHIC ACID;N-Boc-7-aminoenanthic Acid;7-(BOC-AMINO)HEPTANOIC ACID;N-BOC-7-AMINOHEPTANOIC ACID;Boc-L-7-amino-Heptanoicacid
CBNumber
CB4190620
Molecular Formula
C12H23NO4
Formula Weight
245.32
MOL File
60142-89-4.mol
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BOC-7-AMINO-HEPTANOIC ACID Property

Melting point:
56-60 °C
Boiling point:
393.1±25.0 °C(Predicted)
Density 
1.050±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
soluble in Methanol
form 
powder to crystaline
pka
4.77±0.10(Predicted)
color 
White to Almost white
BRN 
2050867
CAS DataBase Reference
60142-89-4(CAS DataBase Reference)
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Safety

Hazard Codes 
Xi
WGK Germany 
3
9-21
HS Code 
2922.50.5000
HazardClass 
IRRITANT
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
15295
Product name
Boc-7-Ahp-OH
Purity
≥99.0% (T)
Packaging
2.5g
Price
$297
Updated
2024/03/01
TCI Chemical
Product number
B4292
Product name
N-(tert-Butoxycarbonyl)-7-aminoheptanoic Acid
Purity
>98.0%(GC)(T)
Packaging
1g
Price
$54
Updated
2024/03/01
TCI Chemical
Product number
B4292
Product name
N-(tert-Butoxycarbonyl)-7-aminoheptanoic Acid
Purity
>98.0%(GC)(T)
Packaging
5g
Price
$157
Updated
2024/03/01
Usbiological
Product number
236056
Product name
Boc-7-aminoheptanoic acid 99+%
Packaging
1g
Price
$179
Updated
2021/12/16
TRC
Product number
B619668
Product name
Boc-7-AminoheptanoicAcid
Packaging
10mg
Price
$45
Updated
2021/12/16
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BOC-7-AMINO-HEPTANOIC ACID Chemical Properties,Usage,Production

Description

Boc-7-Aminoheptanoic acid can be used as a PROTAC linker in the synthesis of PROTACs and other conjugation applicaitons. Boc-7-Aminoheptanoic acid is an alkane chain with terminal carboxlic acid and Boc-protected amino groups. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine.

BOC-7-AMINO-HEPTANOIC ACID Preparation Products And Raw materials

Raw materials

Preparation Products

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BOC-7-AMINO-HEPTANOIC ACID Suppliers

TCI Europe
Tel
320-37350700
Fax
+32 (0)37350701
Email
sales@tcieurope.eu
Country
Europe
ProdList
23671
Advantage
75

60142-89-4, BOC-7-AMINO-HEPTANOIC ACIDRelated Search:


  • BOC-AHEPT-OH
  • BOC-7-AHP-OH
  • BOC-7-AMINO-HEPTANOIC ACID
  • BOC-NH-(CH2)6-COOH
  • N-TERT-BUTYLOXYCARBONYL-7-AMINOHEPTANOIC ACID
  • 7-(BOC-AMINO)ENANTHIC ACID
  • 7-(BOC-AMINO)HEPTANOIC ACID
  • 7-amino-2-[(2-methylpropan-2-yl)oxy-oxomethyl]heptanoic acid
  • N-T-BUTOXYCARBONYL-7-AMINOENANTHIC ACID
  • N-T-BUTOXYCARBONYL-7-AMINOHEPTANOIC ACID
  • N-BOC-7-AMINOHEPTANOIC ACID
  • 7-Aminoheptanoic acid, N-BOC protected
  • Boc-7-AMinoheptanoic acid Boc-7-AMinoheptanoic acid
  • N-tert-Butoxycarbonyl-7-aminoheptanoic acid
  • 7-(Boc-amino)enanthic acid, 7-(Boc-amino)heptanoic acid, Boc-7-aminoheptanoic acid
  • Boc-7-aminoheptanoic acid99%
  • (Tert-Butoxy)Carbonyl 7-Amino-heptanoic acid
  • 7-[(2-methylpropan-2-yl)oxycarbonylamino]heptanoic acid
  • N-(tert-Butoxycarbonyl)-7-aminoheptanoic Acid &gt
  • Heptanoic acid, 7-[[(1,1-dimethylethoxy)carbonyl]amino]-
  • Boc-7-aminoheptanoicaci
  • 7-(tert-Butoxycarbonylamino)enanthic Acid
  • N-(tert-Butoxycarbonyl)-7-aminoenanthic Acid
  • N-Boc-7-aminoenanthic Acid
  • BOC-7-AMINO-HEPTANOIC ACID USP/EP/BP
  • Boc-L-7-amino-Heptanoicacid
  • 7-(tert-butyloxycarbonylamino)-heptanoic acid
  • 60142-89-4
  • C12H23NO4
  • Unnatural Amino Acid Derivatives
  • Specialty Synthesis
  • Peptide Synthesis
  • Linear Core Amino Acids
  • Unusual amino acids