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2-hydroxypropyl dihydrogen phosphate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10602-14-9

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10602-14-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10602-14-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,6,0 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10602-14:
(7*1)+(6*0)+(5*6)+(4*0)+(3*2)+(2*1)+(1*4)=49
49 % 10 = 9
So 10602-14-9 is a valid CAS Registry Number.

10602-14-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxypropyl dihydrogen phosphate

1.2 Other means of identification

Product number -
Other names DL-1-Deoxyglycerol 3-phosphate

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:10602-14-9 SDS

10602-14-9Relevant academic research and scientific papers

A novel method for the synthesis of acetyl phosphate

Devedjiev, Ivan

, p. 1785 - 1787 (2006)

A facile method for the synthesis of acetyl phosphate by a reaction of 2-hydroxypropylphosphate with acetic acid is described. Copyright Taylor & Francis Group, LLC.

Regioselective phosphorylation of carbohydrates and various alcohols by bacterial acid phosphatases; probing the substrate specificity of the enzyme from Shigella flexneri

Van Herk, Teunie,Hartog, Aloysius F.,Van Der Burg, Alida M.,Wever, Ron

, p. 1155 - 1162 (2007/10/03)

Bacterial non-specific acid phosphatases normally catalyze the dephosphorylation of a variety of substrates. As shown previously the enzymes from Shigella flexneri and Salmonella enterica are also able to catalyze the phosphorylation of inosine to inosine monophosphate and D-glucose to D-glucose 6-phosphate (D-G6P) using cheap pyrophosphate as the phosphate donor. After optimization high yields (95%) are achieved in the latter reaction and we show here that it is possible to use these enzymes in a preparative manner. This prompted us to investigate by using 31P NMR and HPLC also the phosphorylation of a broad range of carbohydrates and alcohols. Many cyclic carbohydrates are phosphorylated in a regioselective manner. Non-cyclic carbohydrates are phosphorylated as well. Phosphorylation of linear alcohols, cyclic and aromatic alcohols is also possible. In all cases the acid phosphatase from Shigella prefers a primary alcohol function above a secondary one. We conclude that these enzymes are an attractive alternative to existing chemical and enzymatic methods in the phosphorylation of a broad range of compounds.

Metal ion induced allosteric transition in the catalytic activity of an artificial phosphodiesterase

Takebayashi, Shinji,Ikeda, Masato,Takeuchi, Masayuki,Shinkai, Seiji

, p. 420 - 421 (2007/10/03)

An artificial phosphodiesterase (1) bearing two kinds of metal binding sites, a catalytic site and a regulatory bipyridine site showed a unique allosteric transition in the catalytic activity against the metal concentration.

Plasmid relaxation induced by copper metalated diglycine conjugates under heterogeneous reaction conditions

Madhavaiah,Verma, Sandeep

, p. 923 - 926 (2007/10/03)

This paper reports synthesis and plasmid modification activities of a new class of insoluble copper-metalated diglycine conjugates, containing aliphatic linkers of varying length. Besides providing significant rate enhancement for model phosphate ester cl

A Mechanistic Characterization of the Spontaneous Ring Opening Process of Epoxides In Aqueous Solution: Kinetic and Product Studies

Pocker, Y.,Ronald, B. P.,Anderson, K. W.

, p. 6492 - 6497 (2007/10/02)

A careful determination of the extent of rearrangement during epoxide hydration was carried out in conjunction with nuclear magnetic resonance kinetic studies for both propylene and isobutylene oxides.The complete pH-rate profile was mapped at ionic strength 2.0, and solvent kinetic isotope effects were determined for several limbs.Spectrophotometric analysis of the quantity of aldehyde formed by rearrangement in both the acidic and spontaneous limbs reveals that ionic strength has a profound effect.At ionic strength zero, more rearrangement product is generated in the acidic limb, whereas at ionic strength 2.0, larger amounts of aldehyde are formed in both regions.These results support the conclusion that a different carbocationic intermediate exists in the reaction mechanism for the acidic and spontaneous regions.The experimental observations of the spontaneous region can be explained by the existence of zwitterionic intermediate III.Observed solvent kinetic isotope effects, kH3O+/kD3O+, kHspon/kDspon, of 0.33+/-0.02, 1.78+/-0.25 and 0.35+/-0.03, 1.48+/-0.27 for propylene and isobutylene oxides, respectively, were dissected into components on the basis of classical product studies.At high ionic strength, isolation of compound I, an isobutyraldehyde isobutylene glycol acetal, supports the existence of intermediate III.Apparent partitioning ratios for both the β-hydroxy carbocation, II, and the zwitterion, III, are examined and contrasted.Detailed mechanistic proposals are advanced, and their congruence with a variety of observations described previously in this journal is outlined.

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