Trimethylsilylmethyl Azide

HCID 150751CAS 87576-94-1

Basic information

Standard SMILES
C[Si](C)(C)CN=[N+]=[N-]
InChIKey
HKBUFTCADGLKAS-UHFFFAOYSA-N
Molecular formula
C4H11N3Si
Average molar mass
129.24 g/mol
Monoisotopic mass
129.07222388

Names & identifiers

Preferred name
Trimethylsilylmethyl Azide
IUPAC
azidomethyl(trimethyl)silane
English name
Trimethylsilylmethyl azide
Molecular formula
C4H11N3Si
Molecular weight
129.24

Names & synonyms

Trimethylsilylmethyl azide87576-94-1CCRIS 8030DTXSID40236487RefChem:191819DTXCID40158978677-362-7(azidomethyl)trimethylSilaneAzidomethyltrimethylsilaneSilane, (azidomethyl)trimethyl-azidomethyl(trimethyl)silaneMFCD00059964
Show more names
DK939DKSI087RIMETHYLSILYLMETHYL AZIDE
T1184trimethylsilylmethylazideC4H11N3Si(azidomethyl)(trimethyl)silaneazidomethyl-trimethyl-silaneDKFELEX0251Silyl Methyl azide triMethyl(Azidomethyl)trimethyl-silane

Database identifiers

CAS
87576-94-1
PubChem CID
150751
DTXSID
DTXSID40236487
EC Number
677-362-7
Nikkaji
J209.036H

Properties

Computed structural properties

Topological polar surface area
14.4 Ų
Hydrogen bond donors
0
Hydrogen bond acceptors
2
Rotatable bonds
2
Heavy atoms
8

Physicochemical properties

Boiling point
92 · 92-95°C
Density
0 · 0,87 g/cm3
refractive index
1.43 to · 1.4300 to 1.4340
Flash point
6 °C · 6°C
solubility
Sol organic solvents; insol water.
form
clear liquid

Safety & regulation

GHS classification

GHS Classification · 4 items

Danger

H225 (100%): Highly Flammable liquid and vapor [Danger Flammable liquids]

P210, P233, P240, P241, P242, P243, P280, P303+P361+P353, P370+P378, P403+P235, and P501 (click each P-code to see the statement)

The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.

Hazard information

Hazard Classes and CategoriesFlam. Liq. 2 (100%)

Safety data

ridadr
1992
hs_code
2931900090
risk_code
11-23/24/25
Signal word
Danger
Symbol(GHS)
GHS02
safety_code
16-36/37/39-45

Chemistry & industry

Applications

UsesTrimethylsilylmethyl Azide is used in the amination of organometallic compounds; preparation of heterocyclic compounds; precursor of azomethine ylide, reactant in Silylmethyl-Substituted Heterocumulenes and [3 + 2] Cycloaddition etc.

Preparation methods

PreparationObtained in high yield by reaction of sodium azide and (chloromethyl)trimethylsilane in DMF or HMPA at 80°C.

Suppliers50 total

梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
湖北永阔科技有限公司027-59223108 15972152991 · [email protected]
Career Henan Chemica Co+86-0371-86658258 +86-13203830695 · [email protected]
Junwee Chemical co., Ltd.+86-571-85808636 +86-13958122542 · [email protected]
Dayang Chem (Hangzhou) Co.,Ltd.+86-0571-88938639 17705817739 · [email protected]

Related reactions

22 records

Linked notes

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