Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

15040

Sigma-Aldrich

Boc-β-(3-benzothienyl)-Ala-OH

≥96.0% (TLC)

Synonym(s):

Boc-3-(3-benzothienyl)-L-alanine

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C16H19NO4S
CAS Number:
154902-51-9
Molecular Weight:
321.39
Beilstein:
7081201
MDL number:
MFCD00237538
UNSPSC Code:
12352209
PubChem Substance ID:
57647273
NACRES:
NA.22

Quality Level

100

Assay

≥96.0% (TLC)

reaction suitability

reaction type: Boc solid-phase peptide synthesis

application(s)

peptide synthesis

SMILES string

CC(C)(C)OC(=O)N[C@@H](Cc1csc2ccccc12)C(O)=O

InChI

1S/C16H19NO4S/c1-16(2,3)21-15(20)17-12(14(18)19)8-10-9-22-13-7-5-4-6-11(10)13/h4-7,9,12H,8H2,1-3H3,(H,17,20)(H,18,19)/t12-/m0/s1

InChI key

MURVSBJYXHTRJQ-LBPRGKRZSA-N

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Sanne Boersma et al.
Cell, 183(7), 1930-1945 (2020-11-15)
RNA viruses are among the most prevalent pathogens and are a major burden on society. Although RNA viruses have been studied extensively, little is known about the processes that occur during the first several hours of infection because of a

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service