2-(BOC-Amino)ethanethiol

Modify Date: 2024-01-01 19:09:55

2-(BOC-Amino)ethanethiol Structure
2-(BOC-Amino)ethanethiol structure
Common Name 2-(BOC-Amino)ethanethiol
CAS Number 67385-09-5 Molecular Weight 177.26
Density 1.049 g/mL at 20ºC(lit.) Boiling Point 68ºC0.3 mm Hg(lit.)
Molecular Formula C7H15NO2S Melting Point N/A
MSDS Chinese USA Flash Point >230 °F
Symbol GHS07
GHS07
Signal Word Warning

 Use of 2-(BOC-Amino)ethanethiol


2-(Boc-amino)ethanethiol (compound 35) is a bifunctional cross-linker that can be used in the synthesis of bifunctional azobenzene glycoconjugates[1].

 Names

Name 2-(BOC-Amino)ethanethiol
Synonym More Synonyms

 2-(BOC-Amino)ethanethiol Biological Activity

Description 2-(Boc-amino)ethanethiol (compound 35) is a bifunctional cross-linker that can be used in the synthesis of bifunctional azobenzene glycoconjugates[1].
Related Catalog
References

[1]. Anne Müller, et al. Synthesis of Bifunctional Azobenzene Glycoconjugates for Cysteine-Based Photosensitive Cross-Linking with Bioactive Peptides. Chemistry. 2015 Sep 21;21(39):13723-31.  

 Chemical & Physical Properties

Density 1.049 g/mL at 20ºC(lit.)
Boiling Point 68ºC0.3 mm Hg(lit.)
Molecular Formula C7H15NO2S
Molecular Weight 177.26
Flash Point >230 °F
Exact Mass 177.08200
PSA 77.13000
LogP 1.83180
Appearance of Characters Viscous Liquid or Low Melting Solid | Clear colorless to yellow
Index of Refraction n20/D 1.474(lit.)

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305 + P351 + P338
Personal Protective Equipment Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
Hazard Codes Xi
Risk Phrases 36/37/38
Safety Phrases 26-36
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2930909090

 Synthetic Route

~97%

2-(BOC-Amino)ethanethiol Structure

2-(BOC-Amino)et...

CAS#:67385-09-5

Literature: Kim, Young Zu; Kim, Jae Pil Synthetic Communications, 2002 , vol. 32, # 10 p. 1601 - 1605

~94%

2-(BOC-Amino)ethanethiol Structure

2-(BOC-Amino)et...

CAS#:67385-09-5

Literature: Arisawa, Mieko; Sugata, Chiyoshi; Yamaguchi, Masahiko Tetrahedron Letters, 2005 , vol. 46, # 36 p. 6097 - 6099

~%

2-(BOC-Amino)ethanethiol Structure

2-(BOC-Amino)et...

CAS#:67385-09-5

Literature: Journal of the Chemical Society, Chemical Communications, , # 24 p. 2571 - 2574

~%

2-(BOC-Amino)ethanethiol Structure

2-(BOC-Amino)et...

CAS#:67385-09-5

Literature: Bioorganic and Medicinal Chemistry Letters, , vol. 19, # 10 p. 2742 - 2746

~%

2-(BOC-Amino)ethanethiol Structure

2-(BOC-Amino)et...

CAS#:67385-09-5

Literature: Simons, Stoney S.; Pons, Michel; Johnson, David F. Journal of Organic Chemistry, 1980 , vol. 45, # 15 p. 3084 - 3088

~%

2-(BOC-Amino)ethanethiol Structure

2-(BOC-Amino)et...

CAS#:67385-09-5

Literature: Journal of the American Chemical Society, , vol. 134, # 2 p. 769 - 772

 Customs

HS Code 2930909090
Summary 2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Articles3

More Articles
Synthesis of Bifunctional Azobenzene Glycoconjugates for Cysteine-Based Photosensitive Cross-Linking with Bioactive Peptides.

Chemistry 21 , 13723-31, (2015)

Azobenzene linker molecules can be utilized to control peptide/protein function when they are ligated to appropriately spaced amino acid side chains of the peptide. This is because the photochemical E...

Rapid and simple preparation of thiol-ene emulsion-templated monoliths and their application as enzymatic microreactors.

Lab Chip 15 , 2162-72, (2015)

A novel, rapid and simple method for the preparation of emulsion-templated monoliths in microfluidic channels based on thiol-ene chemistry is presented. The method allows monolith synthesis and anchor...

A convenient route to thiol terminated peptides for conjugation and surface functionalization strategies.

Bioconjug. Chem. 6 , 323, (1995)

The derivatization of poly(p-(chloromethyl)styrene-co-divinylbenzene) (Merrifield resin) with N-(tert-butoxycarbonyl)-2-aminoethanethiol is presented as a convenient route for the generation of thiol ...

 Synonyms

tert-butyl N-(2-sulfanylethyl)carbamate