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13850-91-4

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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

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

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.

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

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