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Merck
CN

15040

Boc-β-(3-benzothienyl)-Ala-OH

≥96.0% (TLC)

Synonym(s):

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

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About This Item

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

Key Documents

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Product Name

Boc-β-(3-benzothienyl)-Ala-OH, ≥96.0% (TLC)

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

SMILES string

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

InChI key

MURVSBJYXHTRJQ-LBPRGKRZSA-N

assay

≥96.0% (TLC)

reaction suitability

reaction type: Boc solid-phase peptide synthesis

application(s)

peptide synthesis

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
417427/1
414506/1
389457/1
381877/1

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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

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