Cas 618441-01-3,[1-(<i>tert</i>-butyl-dimethyl-silanyloxymethyl)-1-hydroxymethyl-3-phenyl-propyl]-carbamic acid <i>tert</i>-butyl ester

618441-01-3

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Basic information

Product Name: [1-(tert-butyl-dimethyl-silanyloxymethyl)-1-hydroxymethyl-3-phenyl-propyl]-carbamic acid tert-butyl ester
Synonyms: [1-(tert-butyl-dimethyl-silanyloxymethyl)-1-hydroxymethyl-3-phenyl-propyl]-carbamic acid tert-butyl ester
CAS NO:618441-01-3
Molecular Formula:
Molecular Weight: 409.641
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: [1-(tert-butyl-dimethyl-silanyloxymethyl)-1-hydroxymethyl-3-phenyl-propyl]-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [1-(tert-butyl-dimethyl-silanyloxymethyl)-1-hydroxymethyl-3-phenyl-propyl]-carbamic acid tert-butyl ester(618441-01-3)
EPA Substance Registry System: [1-(tert-butyl-dimethyl-silanyloxymethyl)-1-hydroxymethyl-3-phenyl-propyl]-carbamic acid tert-butyl ester(618441-01-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 618441-01-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 618441-01-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,8,4,4 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 618441-01:
(8*6)+(7*1)+(6*8)+(5*4)+(4*4)+(3*1)+(2*0)+(1*1)=143
143 % 10 = 3
So 618441-01-3 is a valid CAS Registry Number.

618441-01-3Upstream product

618441-01-3Downstream Products

618441-01-3Relevant academic research and scientific papers

A New Method for the Stereoselective Synthesis of α-Substituted Serine Amino Acid Analogues

Lane, Jonathan W.,Halcomb, Randall L.

, p. 4017 - 4020 (2007/10/03)

(Equation presented) A new method was developed for the stereoselective synthesis of α-substituted serine amino acids. The strategy utilizes a common enantiomerically enriched intermediate obtained through an enzymatic desymmetrization. A variety of amino

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