ChemicalBook > CAS DataBase List > 1,4-BIS-BOC-1,4,7-TRIAZAHEPTANE
1,4-BIS-BOC-1,4,7-TRIAZAHEPTANE
- Product Name
- 1,4-BIS-BOC-1,4,7-TRIAZAHEPTANE
- CAS No.
- 120131-72-8
- Chemical Name
- 1,4-BIS-BOC-1,4,7-TRIAZAHEPTANE
- Synonyms
- 1,4-BIS-BOC-1,4,7-TRIAZAHEPTANE;TERT-BUTYL (2-AMINOETHYL)(2-((TERT-BUTOXYCARBONYL)AMINO)ETHYL)CARBAMATE;tert-butyl N-(2-aminoethyl)-N-[2-[(2-methylpropan-2-yl)oxycarbonylamino]ethyl]carbamate;Carbamic acid, N-(2-aminoethyl)-N-[2-[[(1,1-dimethylethoxy)carbonyl]amino]ethyl]-, 1,1-dimethylethyl ester
- CBNumber
- CB3230558
- Molecular Formula
- C14H29N3O4
- Formula Weight
- 303.4
- MOL File
- 120131-72-8.mol
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Safety
- HS Code
- 29225090
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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
Usbiological
- Product number
- 265938
- Product name
- 1,4-bis-Boc-1,4,7-triazaheptane
- Packaging
- 250mg
- Price
- $368
- Updated
- 2021/12/16
TRC
- Product number
- B404960
- Product name
- 1,4-Bis-boc-1,4,7-triazaheptane
- Packaging
- 25mg
- Price
- $50
- Updated
- 2021/12/16
Iris Biotech GmbH
- Product number
- BNN1080
- Product name
- 1,4-Bis-Boc-1,4,7-triazaheptane
- Packaging
- 500mg
- Price
- $121.5
- Updated
- 2021/12/16
Biosynth Carbosynth
- Product number
- FB52590
- Product name
- 1,4-bis-Boc-1,4,7-triazaheptane
- Packaging
- 250mg
- Price
- $140
- Updated
- 2021/12/16
Iris Biotech GmbH
- Product number
- BNN1080
- Product name
- 1,4-Bis-Boc-1,4,7-triazaheptane
- Packaging
- 1g
- Price
- $189
- Updated
- 2021/12/16
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1,4-BIS-BOC-1,4,7-TRIAZAHEPTANE Chemical Properties,Usage,Production
Description
1,4-Bis-Boc-1,4,7-triazaheptane is a PEG derivative containing an amino group with two Boc-protected amino groups. The amino group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. The Boc group can be deprotected under mild acidic conditions to form the free amine.
Chemical Properties
White powder
1,4-BIS-BOC-1,4,7-TRIAZAHEPTANE Preparation Products And Raw materials
Raw materials
Preparation Products
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1,4-BIS-BOC-1,4,7-TRIAZAHEPTANE Suppliers
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