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37929-85-4

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37929-85-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37929-85-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,9,2 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 37929-85:
(7*3)+(6*7)+(5*9)+(4*2)+(3*9)+(2*8)+(1*5)=164
164 % 10 = 4
So 37929-85-4 is a valid CAS Registry Number.

37929-85-4SDS

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 N-methyl-N-(2-phenylethyl)prop-2-en-1-amine

1.2 Other means of identification

Product number -
Other names Benzeneethanamine,N-methyl-N-2-propenyl

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:37929-85-4 SDS

37929-85-4Downstream Products

37929-85-4Relevant articles and documents

Efficient synthesis of tertiary amines from secondary amines

Kurosu, Michio,Dey, Sevendu Sekhar,Crick, Dean C.

, p. 4871 - 4875 (2007/10/03)

Reliable N-alkylations of secondary amines have been developed. By using DIAD and TPP (or PS-TPP) a variety of secondary amines can be converted to the corresponding tertiary amines in good to excellent yields with diverse alkylhalides; no formation of quaternary amine salts are observed. These protocols are amenable to combinatorial chemistry libraries, and are also useful for the syntheses of secondary amines by an acid lysis of the cleavable tertiary amino resins.

Synthesis of tertiary amines using a polystyrene (REM) resin

Brown, Angus R.,Rees, David C.,Rankovic, Zoran,Morphy, J. Richard

, p. 3288 - 3295 (2007/10/03)

A range of tertiary amines was constructed using a 'traceless' linker on a polystyrene resin (REM resin), starting from seconday amines, primary amines, and resin-bound 'ammonia'. The methodology is characterized by three essential steps conducted under ambient conditions: (1) coupling of the starting amine (Michael addition) to the resin, (2) activation (quaternization), and (3) cleavage of the product amine (Hofmann elimination). The linker is compatible with both acid and base sensitive protecting group strategies. The nature of the chemistry ensures that the tertiary amine products are obtained in consistently high purity (95% or greater). After cleavage of the product, REM resin is regenerated and can be reused for repeat syntheses. The yield and purity of repeat batches is maintained over 5 cycles, allowing the automated synthesis of >0.5 g quantities of pure tertiary amine.

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