106358-02-5

• 

• Basic information

  1. Product Name: D-MYO-INOSITOL 2,4-BIS-PHOSPHATE AMMONIUM SALT
  2. Synonyms: INS(2,4)P2, 4NH4;D-MYO-INOSITOL 2,4-BIS-PHOSPHATE AMMONIUM SALT;D-MYO-INOSITOL 2,4-BISPHOSPHATE, TETRAAMMONIUM SALT;D-myo-inositol-2,4-bis-phosphate*ammonium
  3. CAS NO:106358-02-5
  4. Molecular Formula: C6H26N4O12P2
  5. Molecular Weight: 408.24
  6. EINECS: N/A
  7. Product Categories: Carbohydrates;Carbohydrates A to;Carbohydrates H-LBiochemicals and Reagents;Monosaccharide
  8. Mol File: 106358-02-5.mol
  9. Article Data: 5

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 839.5°C at 760 mmHg
  3. Flash Point: 461.5°C
  4. Appearance: /
  5. Density: N/A
  6. Vapor Pressure: 9.67E-33mmHg at 25°C
  7. Refractive Index: N/A
  8. Storage Temp.: −20°C
  9. Solubility: N/A
  10. CAS DataBase Reference: D-MYO-INOSITOL 2,4-BIS-PHOSPHATE AMMONIUM SALT(CAS DataBase Reference)
  11. NIST Chemistry Reference: D-MYO-INOSITOL 2,4-BIS-PHOSPHATE AMMONIUM SALT(106358-02-5)
  12. EPA Substance Registry System: D-MYO-INOSITOL 2,4-BIS-PHOSPHATE AMMONIUM SALT(106358-02-5)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany: 3
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 106358-02-5(Hazardous Substances Data)

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• SDS
• Upstream product
• Downstream Products
• Article

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106358-02-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106358-02-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,3,5 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 106358-02:
(8*1)+(7*0)+(6*6)+(5*3)+(4*5)+(3*8)+(2*0)+(1*2)=105
105 % 10 = 5
So 106358-02-5 is a valid CAS Registry Number.

InChI:InChI=1/C6H14O12P2.4H3N/c7-1-2(8)5(17-19(11,12)13)4(10)6(3(1)9)18-20(14,15)16;;;;/h1-10H,(H2,11,12,13)(H2,14,15,16);4*1H3/t1-,2-,3+,4-,5-,6-;;;;/m0..../s1

106358-02-5SDS

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	azane,[(1S,2R,4S,5S)-2,3,4,6-tetrahydroxy-5-phosphonooxycyclohexyl] dihydrogen phosphate

1.2 Other means of identification

Product number	-
Other names	D-myo-Inositol 2,4-bisphosphate ammonium salt

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:106358-02-5 SDS

106358-02-5Upstream product

• 98-88-4 benzoyl chloride 
• 956116-98-6 D-1,2:4,5-di-O-isopropylidene-3-O-benzoyl-6-O-benzyl-myo-inositol 
• 956031-41-7 D-1,2-O-isopropylidene-4-O-benzoyl-6-O-benzyl-myo-inositol 
• 956031-37-1 D-1,2-O-isopropylidene-3-O-benzoyl-6-O-benzyl-myo-inositol 
• 956031-43-9 L-1,2-O-isopropylidene-4-O-benzoyl-6-O-benzyl-myo-inositol 
• 956031-39-3 L-1,2-O-isopropylidene-3-O-benzoyl-6-O-benzyl-myo-inositol 
• 956116-99-7 L-1,2:4,5-di-O-isopropylidene-3-O-benzoyl-6-O-benzyl-myo-inositol 
• 114828-09-0 2,4,6-tri-O-benzyl-myo-inositol 1,3-bis(diphenylphosphate) 

106358-02-5Downstream Products

106358-02-5Relevant articles and documents

A Chiral Phosphoramidite Reagent for the Synthesis of Inositol Phosphates

Durantie, Estelle,Huwiler, Samuel,Leroux, Jean-Christophe,Castagner, Bastien

supporting information, p. 3162 - 3165 (2016/07/13)

There is a paucity of chiral phosphoramidite reagents or chiral catalysis methods for the synthesis of biologically relevant inositol phosphates. A new C2-symmetrical chiral phosphoramidite has been developed and successfully applied to the syn

Myo-inositol orthoformates

-

, (2008/06/13)

This invention provides the 4-mono-anion of myo-inositol orthoformate, and describes a process for preparing this anion as well as the use of this anion in the preparation of a variety of mono- and poly-phosphate derivatives of myo-inositol.

Synthesis of myo-Inositol 1,3,4,5-Tetraphosphate and myo-Inositol 1,3-Biphosphate

Billington, David C.,Baker, Raymond

, p. 1011 - 1013 (2007/10/02)

myo-Inositol 1,3,4,5-tetraphosphate, myo-inositol 3,4-biphosphate, and myo-inositol 4-phosphate have been prepared via routes in which a key step is a novel, highly regioselective monooalkylation of myo-inositol orthoformate.

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