Welcome to LookChem.com Sign In|Join Free

CAS

  • or
BOC-N-ME-DL-VAL-OH is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13850-91-4 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 13850-91-4 Structure
  • Basic information

    1. Product Name: BOC-N-ME-DL-VAL-OH
    2. Synonyms: N-ALPHA-T-BUTOXYCARBONYL-N-ALPHA-METHYL-DL-VALINE;BOC-N-METHYL-DL-VALINE;BOC-N-ME-DL-VALINE;BOC-N-ME-DL-VAL-OH;BOC-DL-ME-VAL-OH;2-(tert-butoxycarbonyl(Methyl)aMino)-3-Methylbutanoic acid;N-(tert-Butoxycarbonyl)-N-methyl-DL-valine;N-Boc-N-methyl-DL-valine
    3. CAS NO:13850-91-4
    4. Molecular Formula: C11H21NO4
    5. Molecular Weight: 231.29
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 13850-91-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 322.4oC at 760 mmHg
    3. Flash Point: 148.8oC
    4. Appearance: /
    5. Density: 1.069
    6. Vapor Pressure: 5.74E-05mmHg at 25°C
    7. Refractive Index: 1.466
    8. Storage Temp.: Store at RT.
    9. Solubility: N/A
    10. CAS DataBase Reference: BOC-N-ME-DL-VAL-OH(CAS DataBase Reference)
    11. NIST Chemistry Reference: BOC-N-ME-DL-VAL-OH(13850-91-4)
    12. EPA Substance Registry System: BOC-N-ME-DL-VAL-OH(13850-91-4)
  • 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: 13850-91-4(Hazardous Substances Data)

13850-91-4 Usage

Chemical Properties

White powder

Check Digit Verification of cas no

The CAS Registry Mumber 13850-91-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,5 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13850-91:
(7*1)+(6*3)+(5*8)+(4*5)+(3*0)+(2*9)+(1*1)=104
104 % 10 = 4
So 13850-91-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H21NO4/c1-7(2)8(9(13)14)12(6)10(15)16-11(3,4)5/h7-8H,1-6H3,(H,13,14)

13850-91-4SDS

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 Boc-N-Me-DL-Val-OH

1.2 Other means of identification

Product number -
Other names 3-methyl-2-[methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]butanoic acid

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:13850-91-4 SDS

13850-91-4Relevant articles and documents

Solution-phase synthesis and biological evaluation of triostin A and its analogues

Hattori, Kozo,Koike, Kota,Okuda, Kensuke,Hirayama, Tasuku,Ebihara, Masahiro,Takenaka, Mei,Nagasawa, Hideko

, p. 2090 - 2111 (2016)

Triostin A is a biosynthetic precursor of echinomycin which is one of the most potent hypoxia inducible factor 1 (HIF-1) inhibitors. An improved solution-phase synthesis of triostin A on a preparative scale has been achieved in 17.5% total yield in 13 ste

Total synthesis and biological activity of dolastatin 16

Casalme, Loida O.,Yamauchi, Arisa,Sato, Akinori,Petitbois, Julie G.,Nogata, Yasuyuki,Yoshimura, Erina,Okino, Tatsufumi,Umezawa, Taiki,Matsuda, Fuyuhiko

, p. 1140 - 1150 (2017)

The total synthesis of dolastatin 16, a macrocyclic depsipeptide first isolated from the sea hare Dolabella auricularia as a potential antineoplastic metabolite by Pettit et al., was achieved in a convergent manner. Dolastatin 16 was reported by Tan to ex

Chemical mediators: The remarkable structure and host-selectivity of depsilairdin, a sesquiterpenic depsipeptide containing a new amino acid

Pedras, M. Soledade C.,Chumala, Paulos B.,Wilson Quail

, p. 4615 - 4617 (2004)

(Chemical equation presented) The chemical structure determination of depsilairdin, a highly selective phytotoxin produced by the plant pathogenic fungus Leptosphaeria maculans/Phoma lingam, is described. The elucidation of the unusual chemical structure

Total synthesis of the proposed structure of cyclic hexadepsipeptide veraguamide A

Wang, Dongyu,Jia, Xian,Zhang, Ao

, p. 7027 - 7030 (2012)

We have developed a practical method to assemble the proposed structure of natural product veraguamide A (1) by first preparing the three key fragments followed by optimization of the macrocyclization site. Although the synthetic product gave similar optical rotation to that reported for natural product, significant differences in the 1H and 13C NMR spectra were observed, especially the proton and carbon signals in the two N-MeVal moieties.

Cytotoxic peptides from the marine sponge Cymbastela sp.

Coleman, John E.,Dilip De Silva,Kong, Fangming,Andersen, Raymond J.,Allen, Theresa M.

, p. 10653 - 10662 (1995)

Extracts of the sponge Cymbastela sp. have yielded the novel cytotoxic peptides geodiamolide G (11), hemiasterlin (12), hemiasterlin B (13), criamide A (14) and criamide B (15). The structures of the new compounds were solved via spectroscopic analysis and chemical degradation.

First total synthesis of hoshinoamide A

Liu, Long,Rui, Zihan,Shao, Yutian,Xu, Shengtao,Yang, Yiming,Zhou, Haipin

supporting information, p. 2924 - 2931 (2022/01/12)

Hoshinoamides A, B and C, linear lipopeptides, were isolated from the marine cyanobacterium Caldora penicillata, with potent antiplasmodial activity against chloroquine-sensitive Plasmodium falciparum. Herein, we describe the first total synthesis of hosh

Design, SAR, angiogenic activities evaluation and pro-angiogenic mechanism of new marine cyclopeptide analogs

Li,Lu,Wu,Yu,Xu,Qiu,Pei,Lin,Pang

, p. 1183 - 1194 (2013/07/28)

Angiogenesis plays an important role in a wide range of physiological processes. In this paper, we designed and synthesized a series of new analogs including 11 line-peptides and 9 cyclo-peptides by using a marine cyclopeptide (compound 21) which could st

Total synthesis, absolute configuration, and biological activity of xyloallenoide A

Wang, San-Yong,Xu, Zhong-Liang,Wang, Hui,Li, Chun-Rong,Fu, Li-Wu,Pang, Ji-Yan,Li, Jing,She, Zhi-Gang,Lin, Yong-Cheng

experimental part, p. 973 - 982 (2012/08/08)

The novel natural product xyloallenoide A, isolated from the marine mangrove endophytic fungus from the South China Sea, and its diastereoisomer xyloallenoide A1, which contain N-methyl-substituted amino acids, were synthesized. The absolute configurations of the amino acid units of xyloallenoide A were finally confirmed to be L-Lys, Me-D-Val, and Me-L-Ala. This report represents a practical and attractive alternative for the synthesis of N-methyl-substituted cyclotripeptides. In the preliminary bioassay, synthetic xyloallenoide A showed marginal activities against KB (IC50=9.6 mm) and KBv200 cells (IC50=10.3 μm), and xyloallenoide A1 was inactive against KB and KBv200 cells.

A total synthesis of the ammonium ionophore, (-)-enniatin B

Hu, Dennis X.,Bielitza, Max,Koos, Peter,Ley, Steven V.

supporting information; experimental part, p. 4077 - 4079 (2012/09/07)

A nine-step (longest linear) batch total synthesis of the cyclic hexadepsipeptide (-)-enniatin B is described. The synthesis minimizes precipitation during reaction conditions for adaptability to flow synthesis. The route was used to prepare >100 mg of th

Marine cyclotripeptide X-13 promotes angiogenesis in zebrafish and human endothelial cells via PI3K/Akt/eNOS signaling pathways

Lu, Xi-Lin,Xu, Zhong-Liang,Yao, Xiao-Li,Su, Feng-Juan,Ye, Cheng-Hui,Li, Jing,Lin, Yong-Cheng,Wang, Guang-Lei,Zeng, Jin-Sheng,Huang, Ru-Xun,Ou, Jing-Song,Sun, Hong-Shuo,Wang, Li-Ping,Pang, Ji-Yan,Pei, Zhong

scheme or table, p. 1307 - 1320 (2012/08/08)

Cyclotripeptide X-13 is a core of novel marine compound xyloallenoide A isolated from mangrove fungus Xylaria sp. (no. 2508). We found that X-13 dose-dependently induced angiogenesis in zebrafish embryos and in human endothelial cells, which was accompanied by increased phosphorylation of eNOS and Akt and NO release. Inhibition of PI3K/Akt/eNOS by LY294002 or L-NAME suppressed X-13-induced angiogenesis. The present work demonstrates that X-13 promotes angiogenesis via PI3K/Akt/eNOS pathways.

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 13850-91-4