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1136-21-6

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1136-21-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1136-21-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,3 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1136-21:
(6*1)+(5*1)+(4*3)+(3*6)+(2*2)+(1*1)=46
46 % 10 = 6
So 1136-21-6 is a valid CAS Registry Number.

1136-21-6SDS

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 (3R,4S,5R,6R)-6-(hydroxymethyl)-3,4,5-trimethoxyoxan-2-ol

1.2 Other means of identification

Product number -
Other names Glucopyranose,2,3,4-tri-O-methyl

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:1136-21-6 SDS

1136-21-6Downstream Products

1136-21-6Relevant articles and documents

Characterization of a novel polysaccharide with anti-colon cancer activity from Lactobacillus helveticus MB2-1

Li, Wei,Tang, Weizhi,Ji, Juan,Xia, Xiudong,Rui, Xin,Chen, Xiaohong,Jiang, Mei,Zhou, Jianzhong,Dong, Mingsheng

, p. 6 - 14 (2015/05/13)

The present study aimed at investigating the potential anti-colon cancer activity of three purified exopolysaccharides fractions (LHEPS-1, LHEPS-2 and LHEPS-3) from the Lactobacillus helveticus MB2-1. The experimental evidence showed that LHEPS-1 significantly inhibited cell proliferation of human colon cancer Caco-2 cells in both time- and concentration-dependent manners. In contrast, no significant improvements of the inhibitory effects of LHEPS-2 and LHEPS-3 on Caco-2 cells were observed with increasing sample concentrations or prolonged incubation time. Furthermore, the structure of LHEPS-1 was elucidated using methylated analysis, gas chromatography-mass spectroscopy (GC-MS) and nuclear magnetic resonance spectroscopy (NMR), including one- and two-dimensional nuclear magnetic resonance (1D and 2D NMR). Results indicated that the LHEPS-1 consisted of a decasaccharide repeating unit with the following structure (n≈122): Our results suggested that the LHEPS-1 produced by L. helveticus MB2-1 might be suitable for using as natural anti-colon cancer drugs and functional foods ingredients.

Flavonol glycosides from the leaves of Sterculia urens roxb

Khatoon,Khabiruddin,Asif,Ansari

, p. 287 - 288 (2007/10/02)

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A BITTER MONOTERPENE DIGLYCOSIDE FROM VIBURNUM URCEOLATUM

Iwagawa, Tetsuo,Hase, Tsunao

, p. 255 - 258 (2007/10/02)

From the methanolic extract of the leaves of Viburnum urceolatum a new bitter monoterpen diglycoside, urceolide, has been isolated in addition to several known compounds.The structures were elucidated by spectroscopic and chemical methods.Key Word Index - Viburnum urceolatum; Caprifoliaceae; monoterpene diglycoside; urceolide.

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