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115388-97-1

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115388-97-1 Usage

Chemical Properties

White Crystalline Solid

Uses

Different sources of media describe the Uses of 115388-97-1 differently. You can refer to the following data:
1. Methyl β-L-Daunosamine hydrochloride is used in the synthesis of (L)-Daunosamine and related amino sugars.
2. Methyl β-L-Daunosamine is used in the synthesis of (L)-Daunosamine and related amino sugars.

Check Digit Verification of cas no

The CAS Registry Mumber 115388-97-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,3,8 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 115388-97:
(8*1)+(7*1)+(6*5)+(5*3)+(4*8)+(3*8)+(2*9)+(1*7)=141
141 % 10 = 1
So 115388-97-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H15NO3.ClH/c1-4-7(9)5(8)3-6(10-2)11-4;/h4-7,9H,3,8H2,1-2H3;1H

115388-97-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl β-L-Daunosamine Hydrochloride

1.2 Other means of identification

Product number -
Other names METHYL β-L-DAUNOSAMINIDE HYDROCHLORIDE

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:115388-97-1 SDS

115388-97-1Downstream Products

115388-97-1Relevant articles and documents

SYNTHESIS OF (L)-DAUNOSAMINE AND RELATED AMINO SUGARS

Sammes, Peter G.,Thetford, Dean

, p. 111 - 124 (2007/10/02)

1-(2-Furyl)ethanol (6) has been converted into methyl (+/-)-daunosaminide (1) and methyl (+/-)-ristosaminide (3) by use of an intramolecular cyclisation of a trichloroacetimidate group. (+/-)-Daunosamine (1) has been obtained more directly from the alcohol (10) by use of a modified Mitsunobu reaction; the scope of the latter reaction has been explored using cyclohex-2-en-1-ol as a model substrate.Asymmetric reduction of 2-acetylfuran (5) has given (S)-1-(2-furyl)ethanol (46) in good enantiomeric excess, thus providing a short route to the L-enantiomers of the amino sugars (1), (2), and (3) from a cheap, non-carbohydrate precursor.

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