Welcome to LookChem.com Sign In|Join Free

CAS

  • or
(S)-2-((tert-butoxycarbonyl)amino)-4-(phenylselanyl)butanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1028258-40-3

Post Buying Request

1028258-40-3 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • (S)-2-((tert-butoxycarbonyl)amino)-4-(phenylselanyl)butanoic acid

    Cas No: 1028258-40-3

  • Need to discuss

  • No requirement

  • Adequate

  • Weiyel Inc
  • Contact Supplier

1028258-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1028258-40-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,8,2,5 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1028258-40:
(9*1)+(8*0)+(7*2)+(6*8)+(5*2)+(4*5)+(3*8)+(2*4)+(1*0)=133
133 % 10 = 3
So 1028258-40-3 is a valid CAS Registry Number.

1028258-40-3Relevant articles and documents

The natural product hybrid of Syringolin A and Glidobactin A synergizes proteasome inhibition potency with subsite selectivity

Clerc, Jerome,Li, Nan,Krahn, Daniel,Groll, Michael,Bachmann, Andre S.,Florea, Bogdan I.,Overkleeft, Herman S.,Kaiser, Markus

, p. 385 - 387 (2011)

The preparation of a Syringolin A/Glidobactin A hybrid (SylA-GlbA) consisting of a SylA macrocycle connected to the GlbA side chain and its potent proteasome targeting of all three proteasomal subsites is reported. The influence of the syrbactin macrocycle moiety on subsite selectivity is demonstrated.

DEVELOPMENT OF A SYNTHESIS OF SYRINGOLIN A AND B AND DERIVATIVES THEREOF

-

Page/Page column 5, (2010/02/17)

The synthesis of syringolin A and B and derivatives thereof as well as to pharmaceutical compositions containing the syringolin A or B or derivatives thereof and the use of syringolin A and B and derivatives thereof for prophylaxis and treatment of cancer.

A convenient synthesis of L-α-vinylglycine from L-homoserine lactone

Berkowitz, David B.,Smith, Marianne K.

, p. 39 - 41 (2007/10/03)

A procedure for the synthesis of L-α-vinylglycine from L-homoserine lactone is described. The route developed is convenient (only one chromatography step is required) and efficient (72%; ≥95% optical yield over 4 steps). Key features include the use of acid-labile protecting groups for the amino (Boc) and carboxyl (diphenylmethyl ester) groups, and the use of the phenylselenolate equivalent derived from sodium borohydride and diphenyl diselenide for L-homoserine lactone cleavage.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 1028258-40-3