Structure

Fmoc-Ser-OH

CAS
73724-45-5
Catalog Number
ACM73724455-1
Category
Amino Acids
Molecular Weight
327.33

If you have any other questions or need other size, please get a quote.

  • Product Description
  • Case Study
  • Custom Reviews
  • Custom Q&A
  • Synthetic Use
  • Related Resources

Specification

Description
Useful derivative for the synthesis of phosphoserine peptides by the Fmoc SPPS global phosphorylation methodology.
Synonyms
Fmoc-Ser-OH, N-α-Fmoc-L-serine
InChI
1S/C18H17NO5/c20-9-16(17(21)22)19-18(23)24-10-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,15-16,20H,9-10H2,(H,19,23)(H,21,22)/p-1/t16-/m0/s1
InChI Key
JZTKZVJMSCONAK-INIZCTEOSA-M
Melting Point
80-90℃
Application
Peptide synthesis.
Assay
≥92.0% (acidimetric)
≥98% (TLC)
≥98.0% (HPLC)
Form
powder
Functional Group
hydroxyl
MDL Number
MFCD00051928
Quality Level
200
Reaction Suitability
reaction type: Fmoc solid-phase peptide synthesis
Storage Temperature
2-30℃

Upstream Synthesis Route 1

  • 129460-16-8
  • 71989-33-8
  • 73724-45-5

Reference: [1] Tetrahedron Letters, 2001, vol. 42, # 31, p. 5163 - 5165

Downstream Synthesis Route 1

  • 67-56-1
  • 73724-45-5
  • 82911-78-2

Reference: [1] Arkivoc, 2016, vol. 2017, # 2, p. 260 - 271
[2] Organic letters, 2001, vol. 3, # 16, p. 2477 - 2479

Downstream Synthesis Route 2

  • 73724-45-5
  • 71989-33-8

Reference: [1] Tetrahedron Letters, 1992, vol. 33, # 49, p. 7605 - 7608

* For details of the synthesis route, please refer to the original source to ensure accuracy.

Alfa Chemistry

For product inquiries, please use our online system or send an email to .

Alfa Chemistry
Inquiry Basket
qrcodex
Download
Verification code
* I hereby give my consent that I may receive marketing e-mails with information on existing and new services from this company. I know that I can opt-out from receiving such e-mails at any time or by using the link which will be provided in each marketing e-mail.