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10296-76-1

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10296-76-1 Usage

Uses

Sulfopropanediol can be used as anticorrosive coating based on polyaniline composite microcapsules.

Definition

ChEBI: An alkanesulfonic acid obtained by the formal substitution of one of the methyl hydrogens of propane-1,2-diol by a sulfonic acid group.

Check Digit Verification of cas no

The CAS Registry Mumber 10296-76-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,9 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10296-76:
(7*1)+(6*0)+(5*2)+(4*9)+(3*6)+(2*7)+(1*6)=91
91 % 10 = 1
So 10296-76-1 is a valid CAS Registry Number.
InChI:InChI=1/C3H8O5S/c4-1-3(5)2-9(6,7)8/h3-5H,1-2H2,(H,6,7,8)

10296-76-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-sulfopropanediol

1.2 Other means of identification

Product number -
Other names 2,3-Dihydroxy-propan-1-sulfonsaeure

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:10296-76-1 SDS

10296-76-1Synthetic route

allyl alcohol
107-18-6

allyl alcohol

2,3-dihydroxypropane-1-sulfonic acid
10296-76-1

2,3-dihydroxypropane-1-sulfonic acid

Conditions
ConditionsYield
With sulfuric acid; acetic anhydride; acetic acid
3-monochloro-1,2-propanediol
96-24-2

3-monochloro-1,2-propanediol

2,3-dihydroxypropane-1-sulfonic acid
10296-76-1

2,3-dihydroxypropane-1-sulfonic acid

Conditions
ConditionsYield
With water; sodium sulfite das Natriumsalz entsteht;
3-[5-deoxy-5-(dimethylarsinoyl)-β-D-ribofuranosyloxy]-2-hydroxypropene-1-sulphonic acid
77939-92-5, 358717-87-0

3-[5-deoxy-5-(dimethylarsinoyl)-β-D-ribofuranosyloxy]-2-hydroxypropene-1-sulphonic acid

2,3-dihydroxypropane-1-sulfonic acid
10296-76-1

2,3-dihydroxypropane-1-sulfonic acid

Conditions
ConditionsYield
With hydrogenchloride
sulfuric acid
7664-93-9

sulfuric acid

acetic anhydride
108-24-7

acetic anhydride

acetic acid
64-19-7

acetic acid

allyl alcohol
107-18-6

allyl alcohol

2,3-dihydroxypropane-1-sulfonic acid
10296-76-1

2,3-dihydroxypropane-1-sulfonic acid

Conditions
ConditionsYield
zunaechst unter Eiskuehlung, dann bei 60-70grad;
α-thio-glycerol

α-thio-glycerol

2,3-dihydroxypropane-1-sulfonic acid
10296-76-1

2,3-dihydroxypropane-1-sulfonic acid

Conditions
ConditionsYield
With nitric acid
oxiranyl-methanol
556-52-5

oxiranyl-methanol

2,3-dihydroxypropane-1-sulfonic acid
10296-76-1

2,3-dihydroxypropane-1-sulfonic acid

Conditions
ConditionsYield
Stage #1: oxiranyl-methanol With sodium sulfite In water for 24h; Reflux; Inert atmosphere;
Stage #2:
2,3-dihydroxypropane-1-sulfonic acid
10296-76-1

2,3-dihydroxypropane-1-sulfonic acid

cyclohexylamine
108-91-8

cyclohexylamine

cyclohexylammonium 2,3-dihydroxypropanesulfonate

cyclohexylammonium 2,3-dihydroxypropanesulfonate

Conditions
ConditionsYield
In water58%
2,3-dihydroxypropane-1-sulfonic acid
10296-76-1

2,3-dihydroxypropane-1-sulfonic acid

2-hydroxy-1,3-propanesultone
10200-48-3

2-hydroxy-1,3-propanesultone

Conditions
ConditionsYield
at 140 - 170℃;129 g

10296-76-1Downstream Products

10296-76-1Relevant articles and documents

Comprehensive Synthesis of Substrates, Intermediates, and Products of the Sulfoglycolytic Embden-Meyerhoff-Parnas Pathway

Abayakoon, Palika,Epa, Ruwan,Petricevic, Marija,Bengt, Christopher,Mui, Janice W.-Y.,Van Der Peet, Phillip L.,Zhang, Yunyang,Lingford, James P.,White, Jonathan M.,Goddard-Borger, Ethan D.,Williams, Spencer J.

, p. 2901 - 2910 (2019)

Sulfoglycolysis is a metabolic pathway dedicated to the catabolism of the sulfosugar sulfoquinovose (SQ) into smaller organosulfur fragments. An estimated 10 billion tonnes of SQ fluxes through sulfoglycolysis pathways each year, making it a significant aspect of the biogeochemical sulfur cycle. Delineating the molecular details of sulfoglycolysis requires authentic samples of the various metabolites in these pathways. To this end, we have established chemical and chemoenzymatic methods for the synthesis of the key organosulfur metabolites sulfoquinovosylglycerol, SQ (also in 13C6-labeled form), sulfofructose, sulfofructose-1-phosphate, sulfolactaldehyde, and 2,3-dihydroxypropanesulfonate, as well as an improved route to the chromogenic sulfoquinovosidase substrate 4-nitrophenyl α-sulfoquinovoside.

Arsenic-containing Ribofuranosides: Isolation from Brown Kelp Ecklonia radiata and Nuclear Magnetic Resonance Spectra

Edmonds, John S.,Francesconi, Kevin A.

, p. 2375 - 2382 (2007/10/02)

2-Hydroxy-3-sulphopropyl 5-deoxy-5-(dimethylarsinoyl)-β-ribofuranoside (1a) and 2,3-dihydroxypropyl 5-deoxy-5-(dimethylarsinoyl)-β-ribofuranoside (1b) have been isolated from the brown kelp Ecklonia radiata.Extraction of a second batch of Ecklonia yielded 3-'glycerophosphoryl'-2-hydroxy-1-propane (1c) together with compound (1a).These compounds were identified chiefly by n.m.r. spectroscopy.N.m.r. data for the related (2S)-3--2-hydroxypropyl hydrogen sulphate (1d), extracted from the giant clam Tridacna maxima, are presented also.

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