Cas 276882-72-5,(S)-1-((4S,5R)-5-Hydroxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-butan-1-ol

276882-72-5

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Basic information

Product Name: (S)-1-((4S,5R)-5-Hydroxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-butan-1-ol
Synonyms: (S)-1-((4S,5R)-5-Hydroxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-butan-1-ol
CAS NO:276882-72-5
Molecular Formula:
Molecular Weight: 204.266
EINECS: N/A
Product Categories: N/A
Mol File: 276882-72-5.mol
Article Data: 2

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: (S)-1-((4S,5R)-5-Hydroxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-butan-1-ol(CAS DataBase Reference)
NIST Chemistry Reference: (S)-1-((4S,5R)-5-Hydroxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-butan-1-ol(276882-72-5)
EPA Substance Registry System: (S)-1-((4S,5R)-5-Hydroxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-butan-1-ol(276882-72-5)

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: 276882-72-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 276882-72-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,6,8,8 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 276882-72:
(8*2)+(7*7)+(6*6)+(5*8)+(4*8)+(3*2)+(2*7)+(1*2)=195
195 % 10 = 5
So 276882-72-5 is a valid CAS Registry Number.

276882-72-5Upstream product

276882-72-5Downstream Products

152985-39-2 (-)-pinolidoxin

276882-72-5Relevant articles and documents

Total syntheses of the phytotoxic lactones herbarumin I and II and a synthesis-based solution of the pinolidoxin puzzle

Fuerstner, Alois,Radkowski, Karin,Wirtz, Conny,Goddard, Richard,Lehmann, Christian W.,Mynott, Richard

, p. 7061 - 7069 (2002)

A concise approach to a family of potent herbicidal 10-membered lactones is described on the basis of ring-closing metathesis (RCM) as the key step for the formation of the medium-sized ring. This includes the first total syntheses of herbarumin I (1) and

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