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  • 34897-67-1 Structure
  • Basic information

    1. Product Name: Z-GLU(OSU)-OBZL
    2. Synonyms: Z-L-GLUTAMIC ACID GAMMA-N-HYDROXYSUCCINIMIDE ESTER ALPHA-BENZYL ESTER;Z-GLU(OSU)-OBZL;Z-GLUTAMIC ACID(OSU)-OBZL;Benzyloxycarbonyl-alpha-benzyl-gamma-succinimido-L-glutamate;Z-L-Glu(OSu)-OBzl;Z-L-glutamic acid g-N-hydroxysuccinimide ester a-benzyl ester≥ 98% (HPLC)
    3. CAS NO:34897-67-1
    4. Molecular Formula: C24H24N2O8
    5. Molecular Weight: 468.46
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 34897-67-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: -15°C
    8. Solubility: N/A
    9. CAS DataBase Reference: Z-GLU(OSU)-OBZL(CAS DataBase Reference)
    10. NIST Chemistry Reference: Z-GLU(OSU)-OBZL(34897-67-1)
    11. EPA Substance Registry System: Z-GLU(OSU)-OBZL(34897-67-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 34897-67-1(Hazardous Substances Data)

34897-67-1 Usage

Chemical Properties

White to off-white powder

Check Digit Verification of cas no

The CAS Registry Mumber 34897-67-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,8,9 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 34897-67:
(7*3)+(6*4)+(5*8)+(4*9)+(3*7)+(2*6)+(1*7)=161
161 % 10 = 1
So 34897-67-1 is a valid CAS Registry Number.

34897-67-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Benzyl 5-(2,5-dioxo-1-pyrrolidinyl) N-[(benzyloxy)carbonyl]-L-g lutamate

1.2 Other means of identification

Product number -
Other names Z-Leu-Nle-CHO

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:34897-67-1 SDS

34897-67-1Relevant articles and documents

Evaluation of enzymatic and magnetic properties of γ-glutamyl-[1-13C]glycine and its deuteration toward longer retention of the hyperpolarized state

Elhelaly, Abdelazim Elsayed,Hyodo, Fuminori,Itoda, Marino,Kondo, Yohei,Matsuo, Masayuki,Nishihara, Tatsuya,Nonaka, Hiroshi,Saito, Yutaro,Sando, Shinsuke

, p. 37011 - 37018 (2021/12/07)

Dynamic nuclear polarization (DNP) is an emerging cutting-edge method of acquiring metabolic and physiological information in vivo. We recently developed γ-glutamyl-[1-13C]glycine (γ-Glu-[1-13C]Gly) as a DNP nuclear magnetic resonance (NMR) molecular prob

Protein-Induced Supramolecular Disassembly of Amphiphilic Polypeptide Nanoassemblies

Molla, Mijanur Rahaman,Prasad, Priyaa,Thayumanavan

supporting information, p. 7286 - 7289 (2015/06/30)

Mimicking noncovalent interaction based processes in nature has been an important goal of supramolecular chemistry. Here, we report on amphiphilic polypeptides that self-assemble to form nanoscale supramolecular assemblies and are programmed to disassemble in response to a specific protein. Benzenesulfonamide and carbonic anhydrase have been chosen as the ligand and protein, respectively, to demonstrate this possibility. Since the amphiphilic nanoassembly sequesters hydrophobic guest molecules, the protein-specific disassembly event provides a protein-sensitive molecular release as well. We envision that the binding induced disassembly and guest release might open up new opportunities for the next generation of supramolecular assemblies for protein-specific delivery and diagnostics.

Glutathione based delivery system

-

Page/Page column 4-5, (2008/06/13)

A delivery system. The delivery system includes a carrier or an active compound and a glutathione or a glutathione derivative grafted thereon. The invention also provides a compound including a moiety comprising a vitamin E derivative or a phospholipid de

Glutathione based delivery system

-

Page/Page column 2-3, (2008/06/13)

A delivery system. The delivery system includes a carrier or an active compound and a glutathione or a glutathione derivative grafted thereon. The invention also provides a compound including a moiety comprising a vitamin E derivative or a phospholipid de

Process for and intermediates in the preparation of canfosfamide and its salts

-

Page/Page column 9, (2008/06/13)

A process for and intermediates in the preparation of canfosfamide and its salts. Some of the intermediates have anticancer activity.

Phosphonic acid and phosphinic acid tripeptides as inhibitors of glutathionylspermidine synthetase

Verbruggen, Christophe,De Craecker, Sofie,Rajan, Padinchare,Jiao, Xian-Yun,Borloo, Marianne,Smith, Keith,Fairlamb, Alan H.,Haemers, Achiel

, p. 253 - 258 (2007/10/03)

A series of phosphonic and phosphinic acid derivatives of glutathione were synthesized as potential inhibitors of glutathionylspermidine synthetase, an essential enzyme in the biosynthesis of trypanothione in trypanosomatids. The compounds showed moderate activity. Copyright

Synthesis of amino acids diazoketones

Pettit, Georeg R.,Nelson, Paul S.

, p. 2097 - 2102 (2007/10/02)

A study of carboxylic acid -> diazoketone conversion was pursued employing the γ-carboxyl group of otherwise protected L-glutamic acids.The Arndt-Eistert route employing carboxylic acid chloride intermediates was found best (52percent yield,5b), performed

Synthesis of γ-Glutamyl Peptides Catalyzed by Transamidase from Bacillus natto

Noda, Kosaku,Igata, Keiko,Horikawa, Yoshiko,Fujii, Hisao

, p. 2419 - 2424 (2007/10/02)

Crude ammonium sulfate fraction of a cell free extract from Bacillus natto contained an enzyme (or enzymes) which catalyzed the transamidation reaction specific for glutamine.Both L- and D-isomers of glutamine were active as substrate.On incubation of L- or D-glutamine with the enzyme preparation, two peptides consisting of glutamic acid and glutamine were formed.The main component of the peptides was readily isolated by ion-exchange chromatography and identified as γ-glutamylglutamine by paper chromatography and by paper electrophoresis using authentic peptides.The optical configuration of the amino acid residues in the dipeptide was determined by digestion of the acid hydrolyzate with L-glutamic acid decarboxylase, and the result showed that the dipeptide obtained from L-glutamine was a L-L isomer, while the dipeptide from D-glutamine was a D-D isomer.

Compositions and methods of increasing renal blood flow with gamma-glutamyl amide of dopamine

-

, (2008/06/13)

Covers a γ-glutamyl amide of dopamine selected from the group consisting of EQU1 and a pharmaceutically acceptable acid addition salt thereof. Also covers the use of said γ-glutamyl amide to increase renal blood flow by administering said amide to warm-blooded mammals.

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