tert-Butyl(4-iodobutoxy)diMethylsilane - ≥95% , CAS No.92511-12-1

CAS: 92511-12-1 Cat. No.: T195871 Molecular Weight: 314.28 EC Number: 861-295-7 PubChem CID: 4250746

GRADE & PURITY ≥95%

Synonyms

SY120633 | tert-Butyl(4-iodobutoxy)dimethylsilane, 95% | (4-Iodobutoxy)-t-butyldimethylsilane | FT-0751228 | INGJYKISFRSCQV-UHFFFAOYSA-N | SCHEMBL345800 | (4-iodo-butoxy)-tert-butyl-dimethyl-silane | (4-iodobutoxy)-tert-butyldimethylsilane | 1-(tert-Butyl

Storage

Argon charged,Room temperature

Shipped In

Normal

Overview

Product Describtion:

tert-Butyl(4-iodobutoxy)dimethylsilane is an iodoorganosilane that can be synthesized from tert-butyl(chloro)dimethylsilane.

Product Application:

tert-Butyl(4-iodobutoxy)dimethylsilane may be used as a reagent in the multi-step synthesis of spermine synthon and decanucleotide-spermine conjugates.

Specifications

Synonyms

SY120633 | tert-Butyl(4-iodobutoxy)dimethylsilane, 95% | (4-Iodobutoxy)-t-butyldimethylsilane | FT-0751228 | INGJYKISFRSCQV-UHFFFAOYSA-N | SCHEMBL345800 | (4-iodo-butoxy)-tert-butyl-dimethyl-silane | (4-iodobutoxy)-tert-butyldimethylsilane | 1-(tert-Butyl

Specifications & Purity

≥95%

Storage

Argon charged, Room temperature

Shipped In

Normal

Purity

≥95%

Names and Identifiers

• Pubchem Sid: 504762936
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504762936
• Canonical Smiles: CC(C)(C)[Si](C)(C)OCCCCI
• IUPAC Name: tert-butyl-(4-iodobutoxy)-dimethylsilane
• InChIKey: INGJYKISFRSCQV-UHFFFAOYSA-N
• INCHI: 1S/C10H23IOSi/c1-10(2,3)13(4,5)12-9-7-6-8-11/h6-9H2,1-5H3
• Isomeric SMILES: CC(C)(C)[Si](C)(C)OCCCCI
• PubChem CID: 4250746
• Molecular Weight: 314.28

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organometallic compounds
    • Class Organometalloid compounds
      • Subclass Organosilicon compounds
        • Level5 Organoheterosilanes
          • Level6 Trialkylheterosilanes

• Kingdom: Organic compounds
• Superclass: Organometallic compounds
• Class: Organometalloid compounds
• Subclass: Organosilicon compounds
• Intermediate Tree Nodes: Organoheterosilanes
• Direct Parent: Trialkylheterosilanes
• Alternative Parents: Silyl ethers Organic metalloid salts Organooxygen compounds Organoiodides Hydrocarbon derivatives Alkyl iodides
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Trialkylheterosilane - Silyl ether - Organic metalloid salt - Organic oxygen compound - Hydrocarbon derivative - Organic salt - Organooxygen compound - Organoiodide - Organohalogen compound - Alkyl iodide - Alkyl halide - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as trialkylheterosilanes. These are organoheterosilanes, bearing a silicon atom linked to three alkyl groups and one heteroatom.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Sensitivity: Moisture sensitive.
• Boil Point(°C): 75℃
• Molecular Weight: 314.280 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 6
• Exact Mass: 314.056 Da
• Monoisotopic Mass: 314.056 Da
• Topological Polar Surface Area: 9.200 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 140.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

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