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CAS

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7318-74-3

Boranamine, 1,1-dimethoxy-N,N-dimethyl-, also known as 1,1-dimethoxy-N,N-dimethylboranamine, is an organoborane compound with the chemical formula C3H11BO2N. It is a colorless liquid at room temperature and is soluble in organic solvents. Boranamine, 1,1-dimethoxy-N,N-dimethyl- is a derivative of borane, where one hydrogen atom is replaced by an amine group (NH2), and two methoxy groups (OCH3) are attached to the boron atom. Boranamine, 1,1-dimethoxy-N,N-dimethyl-, is used as a reagent in organic synthesis, particularly in the formation of carbon-boron bonds and as a reducing agent in various chemical reactions. Due to its reactivity and potential toxicity, it should be handled with care and used in well-ventilated areas.

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  • 7318-74-3 Structure

  • Basic information

    1. Product Name: Boranamine, 1,1-dimethoxy-N,N-dimethyl-
    2. Synonyms:
    3. CAS NO:7318-74-3
    4. Molecular Formula: C4H12BNO2
    5. Molecular Weight: 116.956
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 7318-74-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Boranamine, 1,1-dimethoxy-N,N-dimethyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Boranamine, 1,1-dimethoxy-N,N-dimethyl-(7318-74-3)
    11. EPA Substance Registry System: Boranamine, 1,1-dimethoxy-N,N-dimethyl-(7318-74-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 7318-74-3(Hazardous Substances Data)

7318-74-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7318-74-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,1 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7318-74:
(6*7)+(5*3)+(4*1)+(3*8)+(2*7)+(1*4)=103
103 % 10 = 3
So 7318-74-3 is a valid CAS Registry Number.

7318-74-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (dimethylamino)dimethoxy borane

1.2 Other means of identification

Product number -
Other names dimethoxyboranyl-dimethyl-amine

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:7318-74-3 SDS

7318-74-3Downstream Products

7318-74-3Relevant articles and documents

Dialkylamino- and alkoxytrialkylstannanes as reagent for synthesis of organoboryl (trialkylsilyl) ketenes

Nikolaeva, S. N.,Zolotareva, A. S.,Ponomarev, S. V.,Petrosyan, V. S.

, p. 857 - 861 (1994)

Dialkylamino- and alkoxytrialkylstannanes have been studied as N- and O-nucleophilic reagents in substitution reactions at the B-Br bond.The previously unknown bis(dialkylamino)- and dialkoxyboryl trialkylsilyl ketenes were synthesized.Some peculiarities of the reactivity of these compounds have been studied. - Key words: dialkylaminotrialkylstannane, alkoxytrialkylstannane, synthesis; borylsilyl ketene, methanolysis, aminolysis.

Contributions to the Chemistry of Boron, 124. Tris(trimethylsilyl)silyl Boranes and Tris(trimethylsilyl)silyl Borates

Biffar, Werner,Noeth, Heinrich

, p. 1509 - 1515 (2007/10/02)

The reactions of several boron halides, methoxides, alkyls and hydrides with tris(trimethylsilyl)silyllithium, which was isolated as the solvate 3SiLi*3C4H8O, 1 (TMSSLi) have been studied. (CH3)2B-Si3 and 9-3Si-9-BBN, were isolated, while 3Si-B(tC4H9)2 could only be detected by 11B NMR.In addition TMSS-B2, (TMSS)2BNMe2 and (TMSS)2BOCH3 were prepared.The methoxyboranes (CH3)3-nB(OCH3)n add to 1 forming silylborates; however, no OCH3/Si3 substitution occurs.The hydrogen bridge in 9-BBN is cleaved symmetrically.The results can be explained by the basicity and the steric requirements of the TMSS group.The TMSS group exhibits a deshielding effect at the boron nucleus relative to the (CH3)3Si group for silylboranes as well as for silylborates. - Keywords: Silylboranes, Silylborates, Steric effects, 11B NMR Spectra

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