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116786-66-4

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116786-66-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116786-66-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,7,8 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 116786-66:
(8*1)+(7*1)+(6*6)+(5*7)+(4*8)+(3*6)+(2*6)+(1*6)=154
154 % 10 = 4
So 116786-66-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H21NO7/c1-5-7(12-10(17)6(14)3-4-13)8(15)9(16)11(18-2)19-5/h5-9,11,13-16H,3-4H2,1-2H3,(H,12,17)/t5-,6+,7-,8+,9+,11+/m1/s1

116786-66-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 4,6-Dideoxy-4-<(S)-2,4-dihydroxybutanamido>-α-D-mannopyranoside

1.2 Other means of identification

Product number -
Other names Methyl 4,6-Dideoxy-4-((S)-2,4-dihydroxybutanamido)-α-D-mannopyranoside

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:116786-66-4 SDS

116786-66-4Relevant articles and documents

Synthesis and Nuclear Magnetic Resonance Studies of Some N-Acylated Methyl 4-Amino-4,6-dideoxy-α-D-mannopyranosides

Kenne, Lennart,Unger, Per,Wehler, Thomas

, p. 1183 - 1186 (1988)

The methyl α-glycosides of 4-amino-4,6-dideoxy-D-mannopyranose (perosamine), N-acylated with either formic, acetic, or (S)-2,4-dihydroxybutanoic acid, have been synthesized.The (1)H and (13)C n.m.r. spectra of these substances and the parent, non-N-acylated glycoside, demonstrated how the chemical shifts are influenced by the N-acylation.The N-formyl derivative occured in two conformations, s-cis and s-trans, and the free-energy barrier between these, 86.9 kJ mol-1, was defined by dynamic n.m.r. spectroscopy.

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