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24384-87-0

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24384-87-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24384-87-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,8 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 24384-87:
(7*2)+(6*4)+(5*3)+(4*8)+(3*4)+(2*8)+(1*7)=120
120 % 10 = 0
So 24384-87-0 is a valid CAS Registry Number.

24384-87-0SDS

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 6-AMINO-6-DEOXY-1,2-O-ISOPROPYLIDENE-α-D-GLUCOFURANOSE HYDROCHLORIDE

1.2 Other means of identification

Product number -
Other names 6-Amino-6-deoxy-1,2-O-isopropylidene-a-D-glucofuranoseHCl

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:24384-87-0 SDS

24384-87-0Relevant articles and documents

Synthesis, characterization, and antimicrobial activities of novel monosaccharide-containing Schiff base ligands

?etin Telli, Fatma,Astley, Stephen Thomas,Salman, Azize Ye?im

, p. 370 - 380 (2017)

Four new chiral Schiff base ligands (3a–4a, 3b–4b) have been prepared using aminoisopropylidene derivatives of glucose and aminochloralose derivatives of mannose. The synthesized compounds 1 and 2 were characterized by nuclear magnetic resonance (1/

Concise and practical synthesis of (2S,3R,4R,5R) and (2S,3R,4R,5S)-1,6-dideoxy-1,6-iminosugars

Tilekar, Jayant N.,Patil, Nitin T.,Jadhav, Harishchandra S.,Dhavale, Dilip D.

, p. 1873 - 1876 (2007/10/03)

The syntheses of (2S,3R,4R,5R) and (2S,3R,4R,5S)-1,6-dideoxy-1,6 iminosugars 1a and 1b, respectively, from D-glucose are described. The key transformations in this reaction sequence include regio-selective epoxide ring opening with N-benzylamine followed

6-AMINO-6-DEOXY- AND 3-AMINO-3-DEOXY-1,2-O-ISOPROPYLIDENE-α-D-GLUCOFURANOSE 3,5,6-BICYCLOPHOSPHITES

Rumyantseva, S. A.,Koroteev, M. P.,Lysenko, S. A.,Shashkov, A. S.,Nifant'ev, E. E.

, p. 366 - 372 (2007/10/02)

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